Crosstex VH2O2 Chemical Indicators

FDA 510(k) K200096 · Crosstex International, Inc. (A Cantel Medical Company)

Substantially Equivalent

510(k) numberK200096

Submission

Device name
Crosstex VH2O2 Chemical Indicators
Applicant
Crosstex International, Inc. (A Cantel Medical Company)
Rush, NY, US
Received
January 16, 2020
Decision date
July 15, 2021
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JOJ – Indicator, Physical/Chemical Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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K260181LF Process Indicator Tape for Steam SterilizationJOJ · Special Intertape Polymer Group02/20/2026SE
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K250172Green Card Bowie-Dick Test (BD115)JOJ · Special Steritec Products, Inc. (A Getinge Company)02/20/2025SE
K242860Type 5 Integrating Indicator for Steam (CSPN-15)JOJ · Traditional True Indicating, LLC01/17/2025SE
K241036Autoclave Indicator Tape; EO Indicator TapeJOJ · Traditional Jiangmen New Era External Use Drug Co., Ltd.12/17/2024SE
K243475Chemical Indicator for enspire CLCSPS (LCC015)JOJ · Special STERIS Corporation12/04/2024SE
K242795Getinge Assured MI Steam Migrating IntegratorJOJ · Special Steritec Products Mfg. (A Getinge Group Company)10/15/2024SE

Questions and answers

When was Crosstex VH2O2 Chemical Indicators cleared by the FDA?

Crosstex VH2O2 Chemical Indicators (K200096) received a 510(k) decision of Substantially Equivalent on July 15, 2021, 546 days after the submission was received.

What is the product code of K200096?

The FDA product code is JOJ – Indicator, Physical/Chemical Sterilization Process, a Class II (moderate risk) device regulated under 21 CFR 880.2800.