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FDA 510(k)

ONE DIRECTIONAL CLEANING BRUSH

K-Number: K923687 · 1992-09-23

ApplicantEndoscopy Support Services, Inc.
Decision Date1992-09-23
Product CodeFEB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ONE DIRECTIONAL CLEANING BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Endoscopy Support Services, Inc.. It received FDA 510(k) clearance on 1992-09-23 under 510(k) number K923687. 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 ONE DIRECTIONAL CLEANING BRUSH?

ONE DIRECTIONAL CLEANING BRUSH is a medical device that received FDA 510(k) clearance on 1992-09-23. The listed applicant is Endoscopy Support Services, Inc.. The 510(k) number is K923687.

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

ONE DIRECTIONAL CLEANING BRUSH received FDA 510(k) clearance on 1992-09-23, under 510(k) number K923687.

Who is the listed applicant for ONE DIRECTIONAL CLEANING BRUSH?

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

What is the FDA product code for ONE DIRECTIONAL CLEANING BRUSH?

The FDA product code for ONE DIRECTIONAL CLEANING BRUSH is FEB.

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Related Devices (Code: FEB)

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.

K241168System 83 Revolve Endoscope Washer/DisinfectorWassenburg Medical, Inc.K243433enspire 3000 Cleaning and Liquid Chemical Sterilant Processing SystemSTERIS CorporationK230930enspire 3000 Cleaning and Liquid Chemical Sterile Processing SystemSTERIS CorporationK213833SCOPE BUDDY PLUS Endoscope Flushing AidMedivators, Inc.K201920Endoscope Reprocessor OER-EliteOlympus Medical Systems Corp.K173590System 83 Plus Washer/DisinfectorCustom Ultrasonics, Inc.

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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