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FDA 510(k)

VERIFY 3-10 MIN FLASH INTEGRATOR

K-Number: K060066 · 2006-03-24

ApplicantAlbert Browne , Ltd.
Decision Date2006-03-24
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VERIFY 3-10 MIN 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 2006-03-24 under 510(k) number K060066. 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 3-10 MIN FLASH INTEGRATOR?

VERIFY 3-10 MIN FLASH INTEGRATOR is a medical device that received FDA 510(k) clearance on 2006-03-24. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K060066.

When did VERIFY 3-10 MIN FLASH INTEGRATOR receive FDA 510(k) clearance?

VERIFY 3-10 MIN FLASH INTEGRATOR received FDA 510(k) clearance on 2006-03-24, under 510(k) number K060066.

Who is the listed applicant for VERIFY 3-10 MIN 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 3-10 MIN FLASH INTEGRATOR?

The FDA product code for VERIFY 3-10 MIN FLASH INTEGRATOR is JOJ.

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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 LABELK060103ALBERT BROWNE LTD. VERIFY STEAM VALUE INDICATORSK051101VERIFY FLASH INTEGRATORK051056VERIFY 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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