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FDA 510(k)

BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK

K-Number: K932057 · 1994-08-05

ApplicantBoard of Directors, Albert Browne , Ltd.
Decision Date1994-08-05
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK is the device name listed in this FDA 510(k) record. The listed applicant is Board of Directors, Albert Browne , Ltd.. It received FDA 510(k) clearance on 1994-08-05 under 510(k) number K932057. 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 TYPE TEST PACK?

BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK is a medical device that received FDA 510(k) clearance on 1994-08-05. The listed applicant is Board of Directors, Albert Browne , Ltd.. The 510(k) number is K932057.

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

BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK received FDA 510(k) clearance on 1994-08-05, under 510(k) number K932057.

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

The FDA 510(k) record lists Board of Directors, 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 TYPE TEST PACK?

The FDA product code for BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACK is JOJ.

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Other records listing Board of Directors, 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.

K971971BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACKK970918BROWNE STEAM INDICATORK922481BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDEK902958TST CONTROL INTEGRATOR FOR STEAM AUTOCLAVE

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.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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