SIMPSON-ROBERT CORONARY BALLOON DILATATION CATHETE
FDA premarket approval P810046/S053 · decided 1989-03-09
Approval details
- PMA number
- P810046
- Supplement
- S053
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Trade name
- SIMPSON-ROBERT CORONARY BALLOON DILATATION CATHETE
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Applicant
- Advanced Cardiovascular Systems, Inc.
- Date received
- 1989-02-02
- Decision date
- 1989-03-09
- Days to decision
- 35 days
- Decision code
- APPR
- Product code
- LOX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Temecula, CA
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