FDA 510(k), K171993, Zimmon Needle Knife Papillotome
FDA 510(k), K171993, Zimmon Needle Knife Papillotome
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510(K) Number: K171993
Device Name: Zimmon Needle Knife Papillotome
Manufacturer: Wilson-Cook Medical, Inc. / Cook Endoscopy
Device Classification Name: Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Regulation Number: 876.4300
Classification Product Code: KNS
Date Received: 07/03/2017
Decision Date: 08/17/2017
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: Zimmon Needle Knife Papillotome
Manufacturer: Wilson-Cook Medical, Inc. / Cook Endoscopy
Device Classification Name: Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
Regulation Number: 876.4300
Classification Product Code: KNS
Date Received: 07/03/2017
Decision Date: 08/17/2017
Regulation Medical Specialty: Gastroenterology/Urology
- 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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