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FDA 510(k)

CLEANING BRUSH

K-Number: K924103 · 1992-11-16

ApplicantUnited States Endoscopy Group, Inc.
Decision Date1992-11-16
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLEANING BRUSH 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 1992-11-16 under 510(k) number K924103. The device is classified under product code FEB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEANING BRUSH?

CLEANING BRUSH is a medical device that received FDA 510(k) clearance on 1992-11-16. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K924103.

When did CLEANING BRUSH receive FDA 510(k) clearance?

CLEANING BRUSH received FDA 510(k) clearance on 1992-11-16, under 510(k) number K924103.

Who is the listed applicant for CLEANING BRUSH?

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 CLEANING BRUSH?

The FDA product code for CLEANING BRUSH is FEB.

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Related Devices (Code: FEB)

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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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