PMA P830060S028
- Device
- ALTERNATE STERILIZATION/VENTAK(TM)1550,55 PULSE
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S028
- Product code
- LWS
- Decision date
- 1992-10-30
- Classification
- Implantable Cardioverter Defibrillator (non-crt)
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- ALTERNATE STERILIZATION/VENTAK(TM)1550,55 PULSE
- Applicant
- Boston Scientific
- PMA number
- P830060
- Supplement
- S028
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1992-10-30
- Decision code
- APPR
- Date received
- 1991-11-07
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier