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FDA 510(k)

Zimmon Needle Knife Papillotome

K-Number: K171993 · 2017-08-17

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

Related Devices (Code: KNS)

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.