PMA P890061S008
- Device
- VENTAK(R) P MODEL 1600
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S008
- Product code
- LWS
- Decision date
- 1994-08-08
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK(R) P MODEL 1600
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S008
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1994-08-08
- Decision code
- APPR
- Date received
- 1993-10-19
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material