Last synced on 21 February 2025 at 11:05 pm

Right Ventricular Bypass (Assist) Device

Page Type
Product Code
Definition
To provide circulatory support for patients in cardiogenic shock due to acute right ventricular failure.
Physical State
The system is comprised of a blood pump, motor, drive console, flow sensor, and inlet and outlet cannulae. The blood pump is single-use only but the other components can be reused.
Technical Method
The blood pump is driven by a motor and controller, to propel blood from the right ventricle or atrium to the pulmonary circulation.
Target Area
right ventricle or atrium to pulmonary circulation
Review Panel
Cardiovascular
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code OJE to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.

Right Ventricular Bypass (Assist) Device

Page Type
Product Code
Definition
To provide circulatory support for patients in cardiogenic shock due to acute right ventricular failure.
Physical State
The system is comprised of a blood pump, motor, drive console, flow sensor, and inlet and outlet cannulae. The blood pump is single-use only but the other components can be reused.
Technical Method
The blood pump is driven by a motor and controller, to propel blood from the right ventricle or atrium to the pulmonary circulation.
Target Area
right ventricle or atrium to pulmonary circulation
Review Panel
Cardiovascular
Submission Type
HDE - Humanitarian Device Exemption
Device Classification
F
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code OJE to any particular section of the CFR (Code of Federal Regulations). There are multiple reasons why this might be the case:

  • The product code was created for a class III submission that does not follow the normal PMN or PMA path - e.g., for a device that falls under HDE (Humanitarian Device Exemption) or EUA (Emergency Use Authorization).
  • The FDA has generated the product code for an existing Class III device, as a result of a PMA supplement that modifies the device in a way that it can't fit under the existing product code originally assigned
  • The product code was created for internal use at the FDA, and not for classification or regulatory-related purposes.