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FDA 510(k), K960047, BRANNON PEDI PORTSYRINGE
FDA 510(k), K960047, BRANNON PEDI PORTSYRINGE
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510(K) Number: K960047
Device Name: BRANNON PEDI PORTSYRINGE
Manufacturer: JAMES K. BRANNON
Device Classification Name: Syringe, Piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 01/02/1996
Decision Date: 05/24/1996
Regulation Medical Specialty: General Hospital
Device Name: BRANNON PEDI PORTSYRINGE
Manufacturer: JAMES K. BRANNON
Device Classification Name: Syringe, Piston
Regulation Number: 880.5860
Classification Product Code: FMF
Date Received: 01/02/1996
Decision Date: 05/24/1996
Regulation Medical Specialty: General Hospital
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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