FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Over-The-Counter Automated External Defibrillator
PMA: P160029
·
Supplement: S023
·
Decision Jan 5, 2024
Classifications
1
FEI Numbers
8
Registration Numbers
8
Basic Information
- Device Name
- Over-The-Counter Automated External Defibrillator
- Trade Name
- HeartStart OnSite Defibrillator and HeartStart Home Defibrillator
- PMA Number
- P160029
- Supplement Number
- S023
- Device Class
- FDA Class 3
- Product Code
- NSA
- Generic Name
- Over-the-counter automated external defibrillator
- Regulation Number
- 870.5310
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 5, 2024
- Date Received
- January 2, 2024
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
approval for updates to the labeling to comply with California Proposition 65 requirements.
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 |
|---|---|---|---|
| NSA | Over-The-Counter Automated External Defibrillator | FDA class 3 | Cardiovascular |