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FDA 510(k), K022447, BARD ER URETERAL STENT WITH SUTURE
FDA 510(k), K022447, BARD ER URETERAL STENT WITH SUTURE
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510(K) Number: K022447
Device Name: BARD ER URETERAL STENT WITH SUTURE
Manufacturer: C.R. BARD, INC.
Device Classification Name: stent, ureteral
Regulation Number: 876.4620
Classification Product Code: FAD
Date Received: 07/26/2002
Decision Date: 01/23/2003
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: BARD ER URETERAL STENT WITH SUTURE
Manufacturer: C.R. BARD, INC.
Device Classification Name: stent, ureteral
Regulation Number: 876.4620
Classification Product Code: FAD
Date Received: 07/26/2002
Decision Date: 01/23/2003
Regulation Medical Specialty: Gastroenterology/Urology
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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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