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FDA 510(k)

MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION

K-Number: K873265 · 1987-10-28

ApplicantCentral Media
Decision Date1987-10-28
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION is the device name listed in this FDA 510(k) record. The listed applicant is Central Media. It received FDA 510(k) clearance on 1987-10-28 under 510(k) number K873265. 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 MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION?

MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION is a medical device that received FDA 510(k) clearance on 1987-10-28. The listed applicant is Central Media. The 510(k) number is K873265.

When did MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION receive FDA 510(k) clearance?

MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION received FDA 510(k) clearance on 1987-10-28, under 510(k) number K873265.

Who is the listed applicant for MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION?

The FDA 510(k) record lists Central Media as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION?

The FDA product code for MEDIA FOR ANAEROBIC/MICROAERPHILIC ISOLATION is JSI.

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Other records listing Central Media 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.

K873259SPECIALTY MEDIAK873258STREPTOCOCCAL SELECTIVE DIFFEREN. & ENRICHED MEDIAK873257GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.K873260CORYNEBACTERIA ISOLATION MEDIAK873270ACTINOMYCETE DIFFERENTIAL MEDIAK873268MUELLER HINTON MEDIA

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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.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia 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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