One Directional Cleaning Brush

FDA 510(k) K923687 · Endoscopy Support Services, Inc.

Substantially Equivalent

510(k) numberK923687

Submission

Device name
One Directional Cleaning Brush
Applicant
Endoscopy Support Services, Inc.
Paterson, NY, US
Received
July 23, 1992
Decision date
September 23, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
FEB – Accessories, Cleaning, For Endoscope
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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K241168System 83 Revolve Endoscope Washer/DisinfectorFEB · Traditional Wassenburg Medical, Inc.12/19/2024SE
K243433enspire 3000 Cleaning and Liquid Chemical Sterilant Processing SystemFEB · Special STERIS Corporation12/02/2024SE
K230930enspire 3000 Cleaning and Liquid Chemical Sterile Processing SystemFEB · Traditional STERIS Corporation06/30/2023SE
K213833SCOPE BUDDY PLUS Endoscope Flushing AidFEB · Special Medivators, Inc.01/14/2022SE
K201920Endoscope Reprocessor OER-EliteFEB · Special Olympus Medical Systems Corp.09/01/2020SE
K173590System 83 Plus Washer/DisinfectorFEB · Traditional Custom Ultrasonics, Inc.03/30/2020SE
K190969ENDOSCOPE REPROCESSOR OER-EliteFEB · Traditional Olympus Medical Systems Corp.07/09/2019SE
K181472AEROFLEX(TM) Automatic Endoscope Reprocessor with AUTOSURE(TM) MRC MonitorFEB · Traditional Advanced Sterilization Products (Asp)04/23/2019SE
K181865Acu-sInQ Complete Endoscope Cleaning Aid SystemFEB · Traditional STERIS Corporation12/14/2018SE
K172677Advantage Plus Pass-ThruFEB · Traditional Medivators, Inc.12/19/2017SE

Questions and answers

When was One Directional Cleaning Brush cleared by the FDA?

One Directional Cleaning Brush (K923687) received a 510(k) decision of Substantially Equivalent on September 23, 1992, 62 days after the submission was received.

What is the product code of K923687?

The FDA product code is FEB – Accessories, Cleaning, For Endoscope, a Class II (moderate risk) device regulated under 21 CFR 876.1500.