VENTAK 1550 PULSE GENERATOR
FDA premarket approval P830060/S014 · decided 1991-05-17
Approval details
- PMA number
- P830060
- Supplement
- S014
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VENTAK 1550 PULSE GENERATOR
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 1990-02-15
- Decision date
- 1991-05-17
- Days to decision
- 456 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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