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Verify V24 Self-Contained Biological Indicator For Vaporized VH202 Sterilization Processes

by Steris Corporation

510(k) K140499

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK140499 Date17 Jul 2014ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
FRC
Device Class
Class II
Regulation
21 CFR Part 880.2800
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Verify V24 Self-Contained Biological Indicator is a device used to monitor vaporized VH202 sterilization processes. It is designed to provide a self-contained means of verifying the effectiveness of sterilization. The device contains 10^6 colony forming units of Geobacillus stearothermophilus and a specifically formulated growth medium.

The Verify V24 Self-Contained Biological Indicator is supplied for use in monitoring sterilization processes, including those using V-PRO Low Temperature Sterilization Systems and STERRAD sterilizers. It is a single-use device, and its use requires an incubator and the Verify Self-Contained Biological Indicator HP Activator Set. The device has been authorized by the FDA under the 510K clearance type.

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Questions

AI-generated answers, 25 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the Verify V24 used for?

    The Verify V24 is used to monitor vaporized VH202 sterilization processes, providing a self-contained means of verifying sterilization effectiveness.

  • Is the Verify V24 a single-use device?

    Yes, the Verify V24 is a single-use device, requiring an incubator and the Verify Self-Contained Biological Indicator HP Activator Set for use.

  • What type of bacteria does the Verify V24 contain?

    The Verify V24 contains 10^6 colony forming units of Geobacillus stearothermophilus, a specifically formulated growth medium.

  • What is the regulatory status of the Verify V24?

    The Verify V24 has been authorized by the FDA under the 510K clearance type, classified as substantially equivalent.