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FDA 510(k)

VERIFY FLASH INTEGRATOR

K-Number: K051101 · 2005-12-06

ApplicantAlbert Browne , Ltd.
Decision Date2005-12-06
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY FLASH INTEGRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Albert Browne , Ltd.. It received FDA 510(k) clearance on 2005-12-06 under 510(k) number K051101. 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 FLASH INTEGRATOR?

VERIFY FLASH INTEGRATOR is a medical device that received FDA 510(k) clearance on 2005-12-06. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K051101.

When did VERIFY FLASH INTEGRATOR receive FDA 510(k) clearance?

VERIFY FLASH INTEGRATOR received FDA 510(k) clearance on 2005-12-06, under 510(k) number K051101.

Who is the listed applicant for VERIFY FLASH INTEGRATOR?

The FDA 510(k) record lists Albert Browne , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VERIFY FLASH INTEGRATOR?

The FDA product code for VERIFY FLASH INTEGRATOR is JOJ.

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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.

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Other records listing Albert Browne , Ltd. 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.

K063285RELIANCE CI PROCESS INDICATORK061738ALBERT BROWNE LTD. VERIFY STEAM AND EO LOAD RECORD CARDK053479VERIFY DRY HEAT LABELK060066VERIFY 3-10 MIN FLASH INTEGRATORK060103ALBERT BROWNE LTD. VERIFY STEAM VALUE INDICATORSK051056VERIFY SELF-CONTAINED BIOLOGICAL 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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