INTERTACH(R)II & RX2000(R) GRAPHICS PROGRAM MODULE
FDA premarket approval P860007/S009 · decided 1992-12-29
Approval details
- PMA number
- P860007
- Supplement
- S009
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- INTERTACH(R)II & RX2000(R) GRAPHICS PROGRAM MODULE
- Generic name
- PULSE-GENERATOR, SINGLE CHAMBER, SINGLE
- Applicant
- Boston Scientific
- Date received
- 1992-05-11
- Decision date
- 1992-12-29
- Days to decision
- 232 days
- Decision code
- APPR
- Product code
- LWW
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- St Paul, MN
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