PMA P830060S025
- Device
- VENTAK(TM) ECD
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S025
- Product code
- LWS
- Decision date
- 1991-08-12
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK(TM) ECD
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S025
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1991-08-12
- Decision code
- APPR
- Date received
- 1991-05-15
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material