PMA P890061S003
- Device
- VENTAK P MODEL 1600
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S003
- Product code
- LWS
- Decision date
- 1992-05-14
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK P MODEL 1600
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S003
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1992-05-14
- Decision code
- APPR
- Date received
- 1992-04-29
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material