MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD
FDA premarket approval P840068/S014 · decided 1990-08-23
Approval details
- PMA number
- P840068
- Supplement
- S014
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- MODEL 446 & 447 VISTA T,MODEL 940 & 941 VISTA DDD
- Generic name
- Implantable pulse generator, pacemaker (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 1990-07-20
- Decision date
- 1990-08-23
- Days to decision
- 34 days
- Decision code
- APPR
- Product code
- LWP
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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