PMA P890061S006
- Device
- VENTAK P MODEL 6910
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S006
- Product code
- LWS
- Decision date
- 1993-12-14
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK P MODEL 6910
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S006
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1993-12-14
- Decision code
- APPR
- Date received
- 1993-04-15
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material