PMA P890061S001
- Device
- VENTAK P MODELS 1600&1610 & SOFTWARE MODULE 2830
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S001
- Product code
- LWS
- Decision date
- 1992-02-10
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
Current openFDA PMA Record#
- Device
- VENTAK P MODELS 1600&1610 & SOFTWARE MODULE 2830
- Applicant
- Boston Scientific
- PMA number
- P890061
- Supplement
- S001
- Product code
- LWS
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Decision date
- 1992-02-10
- Decision code
- APPR
- Date received
- 1991-05-07
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier