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FDA 510(k)

MODIFIED THAYER-MARTIN AGAR (PLATE)

K-Number: K791425 · 1979-09-17

ApplicantAmerican Laboratory Supply, Inc.
Decision Date1979-09-17
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MODIFIED THAYER-MARTIN AGAR (PLATE) is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791425. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED THAYER-MARTIN AGAR (PLATE)?

MODIFIED THAYER-MARTIN AGAR (PLATE) is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K791425.

When did MODIFIED THAYER-MARTIN AGAR (PLATE) receive FDA 510(k) clearance?

MODIFIED THAYER-MARTIN AGAR (PLATE) received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791425.

Who is the listed applicant for MODIFIED THAYER-MARTIN AGAR (PLATE)?

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

What is the FDA product code for MODIFIED THAYER-MARTIN AGAR (PLATE)?

The FDA product code for MODIFIED THAYER-MARTIN AGAR (PLATE) is JTY.

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Other records listing American Laboratory Supply, 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.

K852578CLED AGARK844929INHIBITORY MOLD AGARK844930BRILLANT GREEN AGARK844931MYCOLOGICAL AGAR W/ANTIBIOTICSK844933BILE ESCULIN AGARK844932MALT AGAR

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Related Devices (Code: JTY)

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.

K210511InTray GCBiomed Diagnostics IncorporatedK993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, 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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