Sterizone Chemical Indicator

FDA 510(k) K141698 · Tso3, Inc.

Substantially Equivalent

510(k) numberK141698

Submission

Device name
Sterizone Chemical Indicator
Applicant
Tso3, Inc.
Vancouver, WA, US
Received
June 24, 2014
Decision date
December 17, 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
JOJ – Indicator, Physical/Chemical Sterilization Process
Device class
Class II (moderate risk)
Regulation
21 CFR 880.2800
Specialty
General Hospital

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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
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More from Steritec Products Mfg. (A Getinge Group Company)

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K173694STERIZONE VP4 SterilizerPJJ · Traditional 03/13/2018SE
K153689STERIZONE SterilizerPJJ · Traditional 06/30/2016SE
K141580Sterizone Self-Contained Biological IndicatorFRC · Traditional 12/17/2014SE
K141163Sterizone SterilizerPJJ · Traditional 12/17/2014SE
K090636TSO3 Ozone Sterilizer, Model 125LFLF · Traditional 12/02/2009SE
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Questions and answers

When was Sterizone Chemical Indicator cleared by the FDA?

Sterizone Chemical Indicator (K141698) received a 510(k) decision of Substantially Equivalent on December 17, 2014, 176 days after the submission was received.

What is the product code of K141698?

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