FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Combination Compression/Decompression Manual Chest Pump With Impedance Respiratory Valve
PMA: P110024
·
Supplement: S006
·
Decision Aug 22, 2024
Classifications
1
FEI Numbers
3
Registration Numbers
3
Basic Information
- Device Name
- Combination Compression/Decompression Manual Chest Pump With Impedance Respiratory Valve
- Trade Name
- ResQCPR System
- PMA Number
- P110024
- Supplement Number
- S006
- Device Class
- FDA Class 3
- Product Code
- PIZ
- Generic Name
- Combination compression/decompression manual chest pump with impedance respiratory valve
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- August 22, 2024
- Date Received
- May 24, 2024
- Supplement Type
- Real-Time Process
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
replacement of the Timing Assist Light (TAL) printed circuit board assembly (PCBA)
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PIZ | Combination Compression/Decompression Manual Chest Pump With Impedance Respiratory Valve | FDA class 3 | Unknown |