Abstract: A percutaneous circulatory support device includes a housing and an impeller disposed within the housing. The impeller is configured to rotate relative to the housing to cause blood to flow through the housing. A motor is operably coupled to the impeller, and the motor is configured to rotate the impeller relative to the housing. A catheter is coupled to the motor. A collar is coupled to the catheter and disposed proximally relative to the housing. The collar includes an internal chamber, and pressure sensor is disposed within the internal chamber of the collar.

Abstract: A percutaneous circulatory support device includes a housing, an impeller disposed within the housing and being rotatable relative to the housing, through the housing, and out of the outlet, a cannula coupled to the housing, the cannula having a body extending between a proximal end and a distal end and along a longitudinal axis, a structural body portion, a surface coating disposed onto the structural body portion of the cannula, and a channel defined between the structural body portion of the cannula and the surface coating, and a pull wire coupled to the cannula and extending through the channel of the cannula. Manipulation of the pull wire causes a change in shape profile of the cannula body.

Abstract: A percutaneous circulatory support device includes a housing and an impeller disposed within the housing and being rotatable relative to the housing to cause blood to flow through the housing. A cannula is coupled to the housing, and a distal tip portion is coupled to the cannula opposite the housing. A control wire is movable to modify at least one of a radius, a stiffness, and a shape of the distal tip portion.

Abstract: A percutaneous circulatory support device includes a housing and an impeller disposed within the housing. The impeller is rotatable relative to the housing to cause blood to flow through the housing. A cannula is coupled to the housing, and a distal tip portion is coupled to the cannula opposite the housing. The distal tip portion includes an inner shaping core configured to maintain a predetermined shape of the distal tip portion and an outer layer disposed outwardly from the inner shaping core or the distal tip portion includes an atraumatic, sphere-shaped distal end.

Abstract: A percutaneous circulatory support device includes a housing, a cannula coupled to the housing, the cannula having a first portion and a second portion, and wherein the cannula includes at least one slot disposed along at least the first portion of the cannula, the at least one slot configured such that the first portion of the cannula is defined by a first stiffness and a second portion of the cannula is defined by a second stiffness, the first stiffness being different than the second stiffness.

Abstract: A percutaneous circulatory support device includes a housing and an impeller disposed within the housing. The impeller is configured to rotate relative to the housing to cause blood to flow through the housing. A motor is operably coupled to the impeller, and the motor is configured to rotate the impeller relative to the housing. A catheter is coupled to the motor, and a pressure sensor is coupled to the catheter and disposed proximally relative to the housing.

Abstract: A catheter system (100) for treating a treatment site (106) within or adjacent to a vessel wall (208A) or a heart valve within a body (107) of a patient (109) includes an energy source (124), a balloon (104), an energy guide (122A), and a tissue identification system (142). The energy source (124) generates energy. The balloon (104) is positionable substantially adjacent to the treatment site (106). The balloon (104) includes a balloon wall (130) that defines a balloon interior (146). The balloon (104) can be configured to retain a balloon fluid (132) within the balloon interior (146). The energy guide (122A) is configured to receive energy from the energy source (124) and guide the energy into the balloon interior (146) so that plasma bubbles (134) are formed in the balloon fluid (132) within the balloon interior (146). The tissue identification system (142) can be configured to acoustically analyze tissue within the treatment site (106).

Abstract: A catheter system (100) for placement within a treatment site (106) at a vessel wall (208A) or a heart valve includes an energy source (124), a balloon (104), an energy guide (122A), and a tissue identification system (142). The energy source (124) generates energy. The balloon (104) is positionable substantially adjacent to the treatment site (106). The balloon (104) has a balloon wall (130) that defines a balloon interior (146). The balloon (104) is configured to retain a balloon fluid (132) within the balloon interior (146). The energy guide (122A) is configured to receive energy from the energy source (124) and guide the energy into the balloon interior (146) so that plasma is formed in the balloon fluid (132) within the balloon interior (146). The tissue identification system (142) is configured to spectroscopically analyze tissue within the treatment site (106).