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FDA 510(k)

VERIFY STEAM Integrating Indicator

K-Number: K243876 · 2025-04-25

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

Device Summary

VERIFY STEAM Integrating Indicator is a medical device manufactured by STERIS Corporation. It received FDA 510(k) clearance on 2025-04-25 under approval 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. It is manufactured by STERIS Corporation. The 510(k) number is K243876.

When was VERIFY STEAM Integrating Indicator approved by the FDA?

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

What company makes VERIFY STEAM Integrating Indicator?

VERIFY STEAM Integrating Indicator is manufactured by STERIS Corporation.

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

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

Other Devices by STERIS Corporation

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Related Devices (Code: JOJ)

Official Source

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