VENTAK P2 AICD SYSTEM
FDA premarket approval P930035/S003 · decided 1995-11-20
Approval details
- PMA number
- P930035
- Supplement
- S003
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- VENTAK P2 AICD SYSTEM
- Generic name
- Implantable cardioverter defibrillator (non-CRT)
- Applicant
- Boston Scientific
- Date received
- 1995-04-06
- Decision date
- 1995-11-20
- Days to decision
- 228 days
- Decision code
- APPR
- Product code
- LWS
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
- Statement
- APPROVAL FOR ALTERNATE MANUFACTURING SITE FOR ASSEMBLY OF EXTERNAL PRODUCTS (PROGRAMMERS, SOFTWAE MDULES/DISKS, EXTERNAL CARDIOVERTER DEFIBRILLATORS, AND RELATED ACCESSORIES) WHICH ARE USED WITH CPI PACEMAKER AND AICD SYSTEMS. THE PROPOSED ALTERNATE MANUFACTURING SITE (CARDIGAN FACILITY) IS LOCATED AT THE FOLLOWING ADDRESS: CPI CARDIGAN FACILITY, 599 CARDIGAN ROAD, SHOREVIEW, MINNESOTA 55126
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