ACS RX ROCKET CORONARY DILATION CATHETER
FDA premarket approval P810046/S188 · decided 1998-06-29
Approval details
- PMA number
- P810046
- Supplement
- S188
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- ACS RX ROCKET CORONARY DILATION CATHETER
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Applicant
- Advanced Cardiovascular Systems, Inc.
- Date received
- 1998-04-16
- Decision date
- 1998-06-29
- Days to decision
- 74 days
- Decision code
- APPR
- Product code
- LOX
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Temecula, CA
- Statement
- Approval for the addition of two quality control tests to the manufacturing process of the ACS RX ROCKET(TM) Coronary dilatation Catheter.
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