Decision Date2017-08-17
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent
Device Summary
Zimmon Needle Knife Papillotome is a medical device manufactured by Wilson-Cook Medical Inc./Cook Endoscopy. It received FDA 510(k) clearance on 2017-08-17 under approval number K171993. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Zimmon Needle Knife Papillotome?
Zimmon Needle Knife Papillotome is a medical device that received FDA 510(k) clearance on 2017-08-17. It is manufactured by Wilson-Cook Medical Inc./Cook Endoscopy. The 510(k) number is K171993.
When was Zimmon Needle Knife Papillotome approved by the FDA?
Zimmon Needle Knife Papillotome received FDA 510(k) clearance on 2017-08-17, under approval number K171993.
What company makes Zimmon Needle Knife Papillotome?
Zimmon Needle Knife Papillotome is manufactured by Wilson-Cook Medical Inc./Cook Endoscopy.
What is the FDA product code for Zimmon Needle Knife Papillotome?
The FDA product code for Zimmon Needle Knife Papillotome is KNS.
Other Devices by Wilson-Cook Medical Inc./Cook Endoscopy
K171607Bronchi and Gastrointestinal Cytology Brush
K172665Classic Cotton Cannulatome®, CannulaTome II® Double Lumen Sphincterotome, Cotton CannulaTome II® PC, UTS® Ultra Taper Sphincterotome, Tri-Tome pc® Triple Lumen Sphincterotome, Howell D.A.S.H.® Sphincterotome with DomeTip®, Billroth II Sphincterotome, Soehendra® BII Sphincterotome, Models ACU-1 and ACU-1-VL active cords
K172288Fusion OMNI Sphincterotome
K190829Gastrointestinal Injection Needles (VIN, LDVI, DVI and MHI)
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K172665Classic Cotton Cannulatome®, CannulaTome II® Double Lumen Sphincterotome, Cotton CannulaTome II® PC, UTS® Ultra Taper Sphincterotome, Tri-Tome pc® Triple Lumen Sphincterotome, Howell D.A.S.H.® Sphincterotome with DomeTip®, Billroth II Sphincterotome, Soehendra® BII Sphincterotome, Models ACU-1 and ACU-1-VL active cordsWilson-Cook Medical Inc./Cook Endoscopy
Official Source
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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.