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FDA 510(k)

PERFRINGENS AGAR BASE

K-Number: K810929 · 1981-04-14

ApplicantOxoid U.S.A., Inc.
Decision Date1981-04-14
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PERFRINGENS AGAR BASE is the device name listed in this FDA 510(k) record. The listed applicant is Oxoid U.S.A., Inc.. It received FDA 510(k) clearance on 1981-04-14 under 510(k) number K810929. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERFRINGENS AGAR BASE?

PERFRINGENS AGAR BASE is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K810929.

When did PERFRINGENS AGAR BASE receive FDA 510(k) clearance?

PERFRINGENS AGAR BASE received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810929.

Who is the listed applicant for PERFRINGENS AGAR BASE?

The FDA 510(k) record lists Oxoid U.S.A., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERFRINGENS AGAR BASE?

The FDA product code for PERFRINGENS AGAR BASE is JSI.

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Other records listing Oxoid U.S.A., Inc. 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.

K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMK884026ESCHERICHIA COLI 0157 LATEX AGGLUTINATION TEST KITK884208LISTERIA SELECTIVE MEDIUM (OXFORD FORMULATION)K874303STAPHYLASE TESTK872956SORBITOL MACCONKEY AGAR NO. 3 CM 813K872135MCBRIDE MEDIUM CM 819

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Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881572XL AGAR BASEAcumedia Manufacturers, Inc.

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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