PORT-A-CATH EPIDURAL SYSTEMS
FDA premarket approval P900052/S009 · decided 2001-10-01
Approval details
- PMA number
- P900052
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- PORT-A-CATH EPIDURAL SYSTEMS
- Generic name
- CATHETER, PERCUTANEOUS, LONG TERM, INTRASPINAL
- Applicant
- Smiths Medical Asd, Inc.
- Date received
- 2001-09-11
- Decision date
- 2001-10-01
- Days to decision
- 20 days
- Decision code
- OK30
- Product code
- LNY
- Advisory committee
- General Hospital
- Expedited review
- No
- Location
- St. Paul, MN
- Statement
- ELIMINATE THE INSPECTION PROCEDURE ON SOME INCOMING COMPONENTS USED IN THE MANUFACTURE OF THE PORT-A-CATH(R) EPIDURAL SYSTEMS.
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