FDA 510(k)

REUSABLE ENDOSCOPIC ACCESSORY HANDLE

K-Number: K961762 · 1996-07-22

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1996-07-22

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

REUSABLE ENDOSCOPIC ACCESSORY HANDLE 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 1996-07-22 under 510(k) number K961762. 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 REUSABLE ENDOSCOPIC ACCESSORY HANDLE?

REUSABLE ENDOSCOPIC ACCESSORY HANDLE is a medical device that received FDA 510(k) clearance on 1996-07-22. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K961762.

When did REUSABLE ENDOSCOPIC ACCESSORY HANDLE receive FDA 510(k) clearance?

REUSABLE ENDOSCOPIC ACCESSORY HANDLE received FDA 510(k) clearance on 1996-07-22, under 510(k) number K961762.

Who is the listed applicant for REUSABLE ENDOSCOPIC ACCESSORY HANDLE?

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 REUSABLE ENDOSCOPIC ACCESSORY HANDLE?

The FDA product code for REUSABLE ENDOSCOPIC ACCESSORY HANDLE is KNS.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.