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FDA 510(k)

VERIFY STEAM Integrating Indicator

K-Number: K243876 · 2025-04-25

ApplicantSTERIS Corporation
Decision Date2025-04-25
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY STEAM Integrating Indicator is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2025-04-25 under 510(k) number K243876. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VERIFY STEAM Integrating Indicator?

VERIFY STEAM Integrating Indicator is a medical device that received FDA 510(k) clearance on 2025-04-25. The listed applicant is STERIS Corporation. The 510(k) number is K243876.

When did VERIFY STEAM Integrating Indicator receive FDA 510(k) clearance?

VERIFY STEAM Integrating Indicator received FDA 510(k) clearance on 2025-04-25, under 510(k) number K243876.

Who is the listed applicant for VERIFY STEAM Integrating Indicator?

The FDA 510(k) record lists STERIS Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERIFY STEAM Integrating Indicator?

The FDA product code for VERIFY STEAM Integrating Indicator is JOJ.

Other records listing STERIS Corporation as applicant

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Related Devices (Code: JOJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K260181LF Process Indicator Tape for Steam SterilizationIntertape Polymer GroupK251991SafeSecure Steam Sterilization Process Indicator (4012, 4013, 4014, 4016); SafeSecure Vaporized Hydrogen Peroxide Sterilization Process Indicator (4211, 4212, 4213)Shenzhen Safesecure Medical Infection Control Tech Co. , Ltd.K251035DISINTEK™ PA Test StripsSerim ResearchK251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118STERIS CorporationK250172Green Card Bowie-Dick Test (BD115)Steritec Products, Inc. (A Getinge Company)K242860Type 5 Integrating Indicator for Steam (CSPN-15)True Indicating, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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