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FDA 510(k)

BROWNE TST SINGLE USE BOWIE-DICK TYPE TEST PACK

K-Number: K971971 · 1998-07-10

ApplicantBoard of Directors, Albert Browne , Ltd.
Decision Date1998-07-10
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 1998-07-10 under 510(k) number K971971. 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 1998-07-10. The listed applicant is Board of Directors, Albert Browne , Ltd.. The 510(k) number is K971971.

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 1998-07-10, under 510(k) number K971971.

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.

K970918BROWNE STEAM INDICATORK932057BROWNE TST SINGLE USE BOWIE DICK TYPE TEST PACKK922481BROWNE 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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