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FDA 510(k)

VERIFY VH202 Indicator Tape

K-Number: K183293 · 2019-01-04

ApplicantSTERIS Corporation
Decision Date2019-01-04
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY VH202 Indicator Tape is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2019-01-04 under 510(k) number K183293. 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 VH202 Indicator Tape?

VERIFY VH202 Indicator Tape is a medical device that received FDA 510(k) clearance on 2019-01-04. The listed applicant is STERIS Corporation. The 510(k) number is K183293.

When did VERIFY VH202 Indicator Tape receive FDA 510(k) clearance?

VERIFY VH202 Indicator Tape received FDA 510(k) clearance on 2019-01-04, under 510(k) number K183293.

Who is the listed applicant for VERIFY VH202 Indicator Tape?

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 VH202 Indicator Tape?

The FDA product code for VERIFY VH202 Indicator Tape 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 CorporationK243876VERIFY STEAM Integrating IndicatorSTERIS CorporationK250172Green Card Bowie-Dick Test (BD115)Steritec Products, Inc. (A Getinge Company)

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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