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FDA 510(k), K033862, BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
FDA 510(k), K033862, BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
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510(K) Number: K033862
Device Name: BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
Manufacturer: BIOTEQUE CORP.
Device Classification Name: stents, drains and dilators for the biliary ducts
Regulation Number: 876.5010
Classification Product Code: FGE
Date Received: 12/12/2003
Decision Date: 02/14/2005
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: BIOTEQ PIGTAIL DRAINAGE CATHETER SET (ONE STEP TYPE) WITH OR WITHOUT SAFETY STRING LOCK
Manufacturer: BIOTEQUE CORP.
Device Classification Name: stents, drains and dilators for the biliary ducts
Regulation Number: 876.5010
Classification Product Code: FGE
Date Received: 12/12/2003
Decision Date: 02/14/2005
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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