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FDA 510(k)

DTM (DERMATOPHYTE TEST MEDIUM) AGAR

K-Number: K791414 · 1979-10-17

ApplicantBiomedia, Inc.
Decision Date1979-10-17
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DTM (DERMATOPHYTE TEST MEDIUM) AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Biomedia, Inc.. It received FDA 510(k) clearance on 1979-10-17 under 510(k) number K791414. 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 DTM (DERMATOPHYTE TEST MEDIUM) AGAR?

DTM (DERMATOPHYTE TEST MEDIUM) AGAR is a medical device that received FDA 510(k) clearance on 1979-10-17. The listed applicant is Biomedia, Inc.. The 510(k) number is K791414.

When did DTM (DERMATOPHYTE TEST MEDIUM) AGAR receive FDA 510(k) clearance?

DTM (DERMATOPHYTE TEST MEDIUM) AGAR received FDA 510(k) clearance on 1979-10-17, under 510(k) number K791414.

Who is the listed applicant for DTM (DERMATOPHYTE TEST MEDIUM) AGAR?

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

What is the FDA product code for DTM (DERMATOPHYTE TEST MEDIUM) AGAR?

The FDA product code for DTM (DERMATOPHYTE TEST MEDIUM) AGAR is JSI.

Related Clinical Trials

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Other records listing Biomedia, 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.

K821300#2010 CAMPHYLOBACTER AGARK821301#50002 QUAD DIAGNOSTIC SYSTEMK821302#50003 QUAD DIAGNOSTIC SYSTEMK821108BI PLATE-XLD/HEKTOEN #30012K811478EMB AGAR, LEVINEK811477MACCONKEY AGAR

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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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