FDA 510(k)

U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT

K-Number: K955248 · 1996-05-21

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1996-05-21

Product CodeKNT

Advisory CommitteeGU

DecisionUnknown

Device Summary

U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1996-05-21 under 510(k) number K955248. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT?

U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT is a medical device that received FDA 510(k) clearance on 1996-05-21. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K955248.

When did U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT receive FDA 510(k) clearance?

U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT received FDA 510(k) clearance on 1996-05-21, under 510(k) number K955248.

Who is the listed applicant for U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT?

The FDA product code for U.S. ENDOSCOPY PULL PEG KIT & U.S. ENDOSCOPY GUIDEWIRE PEG KIT is KNT.

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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.