FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Over-The-Counter Automated External Defibrillator
PMA: P160029
·
Supplement: S026
·
Decision Dec 12, 2024
Classifications
1
FEI Numbers
8
Registration Numbers
8
Basic Information
- Device Name
- Over-The-Counter Automated External Defibrillator
- Trade Name
- HeartStart Home Defibrillator, HeartStart OnSite Defibrillator, HeartStart HS1 SMART Pads, Adult (M5071A), HeartStart HS
- PMA Number
- P160029
- Supplement Number
- S026
- 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
- December 12, 2024
- Date Received
- September 13, 2024
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
material change to pads
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 |