E-Z Check Ozone Test Strips

FDA 510(k) K132344 · Reprocessing Products Corporation (Rpc)

Substantially Equivalent

510(k) numberK132344

Submission

Device name
E-Z Check Ozone Test Strips
Applicant
Reprocessing Products Corporation (Rpc)
Tucson, AZ, US
Received
July 29, 2013
Decision date
February 25, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSY – Strip, Test, Reagent, Residuals For Dialysate, Disinfectant
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5665
Specialty
Gastroenterology, Urology
Life-sustaining
Yes

Other 510(k)s with product code MSY

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K243898Chlorine Sentinel IIMSY · Traditional Nelson Environmental Technologies, Inc.04/11/2025SE
K222167E-Z Chek Chlorine Residual Test Strips (K100-0101B)MSY · Traditional Reprocessing Products Corporation (Rpc)10/18/2022SE
K193169Nelson Sentinel Series Basic Chlorine SentinelMSY · Traditional Nelson Environmental Technologies, Inc.10/29/2020SE
K090338Ultra Low Total Chlorine, E-Z Chek Sensitive Total ChlorineMSY · Traditional Reprocessing Products Corp05/08/2009SE
K080712Serim Hisense Ultra 0.1, Part Number 5167MSY · Traditional Serim Research Corp.05/06/2008SE
K002011Glutartest 1 Reagent StripMSY · Traditional Integrated Biomedical Technology, Inc.01/22/2001SE
K001194Sterichek Total Chlorine Reagent StripsMSY · Traditional Environmental Test Systems, Inc.07/11/2000SE
K994226Sterichek Total Chlorine Reagent StripsMSY · Traditional Environmental Test Systems, Inc.03/22/2000SE
K983997Sterichek Total Chlorine Test KitMSY · Traditional Environmental Test Systems, Inc.04/02/1999SE
K974064Micro X Residual Test StripsMSY · Traditional Reprocessing Products Corp12/07/1998SE

More from Reprocessing Products Corp

510(k)DeviceDecision
K222167E-Z Chek Chlorine Residual Test Strips (K100-0101B)MSY · Traditional 10/18/2022SE

Questions and answers

When was E-Z Check Ozone Test Strips cleared by the FDA?

E-Z Check Ozone Test Strips (K132344) received a 510(k) decision of Substantially Equivalent on February 25, 2014, 211 days after the submission was received.

What is the product code of K132344?

The FDA product code is MSY – Strip, Test, Reagent, Residuals For Dialysate, Disinfectant, a Class II (moderate risk) device regulated under 21 CFR 876.5665.