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FDA 510(k)

BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK

K-Number: K002741 · 2002-07-03

ApplicantAlbert Browne , Ltd.
Decision Date2002-07-03
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK 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 2002-07-03 under 510(k) number K002741. 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 BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK?

BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK is a medical device that received FDA 510(k) clearance on 2002-07-03. The listed applicant is Albert Browne , Ltd.. The 510(k) number is K002741.

When did BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK receive FDA 510(k) clearance?

BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK received FDA 510(k) clearance on 2002-07-03, under 510(k) number K002741.

Who is the listed applicant for BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK?

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 BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK?

The FDA product code for BROWNE TST SINGLE USE BOWIE DICK/INTEGRATOR TEST PACK 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 LABELK060066VERIFY 3-10 MIN FLASH INTEGRATORK060103ALBERT BROWNE LTD. VERIFY STEAM VALUE INDICATORSK051101VERIFY FLASH INTEGRATOR

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Related Devices (Code: JOJ)

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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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