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FDA 510(k)

DSNARE, MODEL 00711087

K-Number: K051637 · 2005-10-31

ApplicantUnited States Endoscopy Group, Inc.
Decision Date2005-10-31
Product CodeFCK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DSNARE, MODEL 00711087 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 2005-10-31 under 510(k) number K051637. The device is classified under product code FCK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSNARE, MODEL 00711087?

DSNARE, MODEL 00711087 is a medical device that received FDA 510(k) clearance on 2005-10-31. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K051637.

When did DSNARE, MODEL 00711087 receive FDA 510(k) clearance?

DSNARE, MODEL 00711087 received FDA 510(k) clearance on 2005-10-31, under 510(k) number K051637.

Who is the listed applicant for DSNARE, MODEL 00711087?

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 DSNARE, MODEL 00711087?

The FDA product code for DSNARE, MODEL 00711087 is FCK.

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Related Devices (Code: FCK)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.

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