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FDA 510(k)

VERIFY 270FP CHALLENGE PACK

K-Number: K103053 · 2011-03-10

ApplicantSTERIS Corporation
Decision Date2011-03-10
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY 270FP CHALLENGE PACK is the device name listed in this FDA 510(k) record. The listed applicant is STERIS Corporation. It received FDA 510(k) clearance on 2011-03-10 under 510(k) number K103053. 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 270FP CHALLENGE PACK?

VERIFY 270FP CHALLENGE PACK is a medical device that received FDA 510(k) clearance on 2011-03-10. The listed applicant is STERIS Corporation. The 510(k) number is K103053.

When did VERIFY 270FP CHALLENGE PACK receive FDA 510(k) clearance?

VERIFY 270FP CHALLENGE PACK received FDA 510(k) clearance on 2011-03-10, under 510(k) number K103053.

Who is the listed applicant for VERIFY 270FP CHALLENGE PACK?

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 270FP CHALLENGE PACK?

The FDA product code for VERIFY 270FP CHALLENGE PACK is JOJ.

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Other records listing STERIS Corporation as applicant

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.

K261055AMSCO 700 Steam SterilizerK251666SYSTEM 1E Liquid Chemical Sterilant Processing System, Model P6700; SYSTEM 1 endo Liquid Chemical Sterilant Processing System, Model P6900K260766Celerity 5 HP Biological Indicator (LCB052)K252680Celerity™ 20 HP Biological IndicatorK251048Rapicide PA High-Level Disinfection Test Strip Model Ref # = ML02-0118K243876VERIFY STEAM Integrating Indicator

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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.

K2619923M™ Attest™ Steam Chemical Integrator (1243A, 1243B, 1243RE, 1243RES)Solventum US, LLCK260181LF 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 Corporation

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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