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FDA 510(k)

SELENITE CYSTINE BROTH BASE

K-Number: K841660 · 1984-05-14

ApplicantOxoid U.S.A., Inc.
Decision Date1984-05-14
Product Code
DecisionSubstantially Equivalent

Device Summary

SELENITE CYSTINE BROTH 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 1984-05-14 under 510(k) number K841660. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SELENITE CYSTINE BROTH BASE?

SELENITE CYSTINE BROTH BASE is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Oxoid U.S.A., Inc.. The 510(k) number is K841660.

When did SELENITE CYSTINE BROTH BASE receive FDA 510(k) clearance?

SELENITE CYSTINE BROTH BASE received FDA 510(k) clearance on 1984-05-14, under 510(k) number K841660.

Who is the listed applicant for SELENITE CYSTINE BROTH BASE?

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

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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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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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