FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Temporary Non-Roller Type Left Heart Support Blood Pump
PMA: P140003
·
Supplement: S098
·
Decision Jul 8, 2022
Classifications
1
FEI Numbers
3
Registration Numbers
3
Basic Information
- Device Name
- Temporary Non-Roller Type Left Heart Support Blood Pump
- Trade Name
- Impella 2.5, Impella CP, Impella CP with SmartAssist
- PMA Number
- P140003
- Supplement Number
- S098
- Device Class
- FDA Class 3
- Product Code
- OZD
- Generic Name
- Temporary non-roller type left heart support blood pump
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- July 8, 2022
- Date Received
- April 15, 2022
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for the updated labeling with the information from the Impella PROTECTED PCI Post-Approval cVAD Registry Study.
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 |
|---|---|---|---|
| OZD | Temporary Non-Roller Type Left Heart Support Blood Pump | FDA class 3 | Unknown |