PMA P830060S013
- Device
- VENTAK 1550 PULSE GENERATOR
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S013
- Product code
- LWS
- Decision date
- 1990-01-04
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK 1550 PULSE GENERATOR
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S013
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1990-01-04
- Decision code
- APPR
- Date received
- 1989-11-20
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier