Last synced on 21 February 2025 at 11:05 pm

Combination Compression/Decompression Manual Chest Pump With Impedance Respiratory Valve

Page Type
Product Code
Definition
Intended for use as a CPR adjunct to improve the likelihood of survival in adult patients with non-traumatic cardiac arrest.
Physical State
The device system is comprised of two components: A manual pump containing a suction cup so that active decompression can take place. The valve is inserted in the respiratory circuit (e.g., facemask or advanced airway) during CPR.
Technical Method
Uses active compression and decompression of the victim's chest during manual CPR, as well as impeding the inflow of air during the decompression phase to reduce the intrathoracic pressure and increase blood flow.
Target Area
The pump is placed on the victim's chest, and the valve is placed within the respiratory circuit.
Review Panel
Cardiovascular
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code PIZ 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.

Combination Compression/Decompression Manual Chest Pump With Impedance Respiratory Valve

Page Type
Product Code
Definition
Intended for use as a CPR adjunct to improve the likelihood of survival in adult patients with non-traumatic cardiac arrest.
Physical State
The device system is comprised of two components: A manual pump containing a suction cup so that active decompression can take place. The valve is inserted in the respiratory circuit (e.g., facemask or advanced airway) during CPR.
Technical Method
Uses active compression and decompression of the victim's chest during manual CPR, as well as impeding the inflow of air during the decompression phase to reduce the intrathoracic pressure and increase blood flow.
Target Area
The pump is placed on the victim's chest, and the valve is placed within the respiratory circuit.
Review Panel
Cardiovascular
Submission Type
PMA
Device Classification
Class 3
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

The FDA has not linked product code PIZ 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.