NOVOSTE(TM) BETA-CATH(TM) SYSTEM
FDA premarket approval P000018/S002 · decided 2000-12-18
Approval details
- PMA number
- P000018
- Supplement
- S002
- Supplement type
- Special (Immediate Track)
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- NOVOSTE(TM) BETA-CATH(TM) SYSTEM
- Generic name
- Intravascular radiation delivery system
- Applicant
- Best Vascular, Inc.
- Date received
- 2000-11-17
- Decision date
- 2000-12-18
- Days to decision
- 31 days
- Decision code
- APPR
- Product code
- MOU
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Norcross, GA
- Statement
- APPROVAL FOR THE ADDITION OF A NEW QUALITY CONTROL TEST METHOD DURING THE MANUFACTURING PROCESS OF THE B-CATH(TM) DELIVERY CATHETER.
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