ACS CONCORFE(TM) CORONARY DILATION BALLOON CATHETER
FDA premarket approval P810046/S158 · decided 1996-02-05
Approval details
- PMA number
- P810046
- Supplement
- S158
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- ACS CONCORFE(TM) CORONARY DILATION BALLOON CATHETER
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Applicant
- Advanced Cardiovascular Systems, Inc.
- Date received
- 1995-09-25
- Decision date
- 1996-02-05
- Days to decision
- 133 days
- Decision code
- APPR
- Product code
- LOX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Temecula, CA
- Statement
- APPROVAL FOR ACS CONCORDE CORONARY DILATATION CATHETER
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