EMC2 Lens Fog Reduction Solution & Cleaning Kit

FDA 510(k) K941134 · H & C Chemical, Inc.

Substantially Equivalent

510(k) numberK941134

Submission

Device name
EMC2 Lens Fog Reduction Solution & Cleaning Kit
Applicant
H & C Chemical, Inc.
Minneapolis, MN, US
Received
March 9, 1994
Decision date
May 16, 1994
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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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
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More from Medivators, Inc.

510(k)DeviceDecision
K941094Insufflation Tubing & FilterHET · Traditional 05/10/1994SE
K9345282C Lens Fog Reduction & Cleaning DeviceGCJ · Traditional 02/16/1994SE

Questions and answers

When was EMC2 Lens Fog Reduction Solution & Cleaning Kit cleared by the FDA?

EMC2 Lens Fog Reduction Solution & Cleaning Kit (K941134) received a 510(k) decision of Substantially Equivalent on May 16, 1994, 68 days after the submission was received.

What is the product code of K941134?

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