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FDA 510(k)

THAYER-MARTIN AGAR

K-Number: K800977 · 1980-05-23

ApplicantQuality Assurance Laboratory, Inc.
Decision Date1980-05-23
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER-MARTIN AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Quality Assurance Laboratory, Inc.. It received FDA 510(k) clearance on 1980-05-23 under 510(k) number K800977. 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 THAYER-MARTIN AGAR?

THAYER-MARTIN AGAR is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Quality Assurance Laboratory, Inc.. The 510(k) number is K800977.

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

THAYER-MARTIN AGAR received FDA 510(k) clearance on 1980-05-23, under 510(k) number K800977.

Who is the listed applicant for THAYER-MARTIN AGAR?

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

What is the FDA product code for THAYER-MARTIN AGAR?

The FDA product code for THAYER-MARTIN AGAR is JTY.

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Other records listing Quality Assurance Laboratory, 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.

K800986TRYPTICASE SOY AGAR W5% SHEEP BLOODK800987MUELLER HINTON AGARK800978XYLOSE LYSINE DESOXYCHOLATE AGARK800981CHOCOLATE AGAR W/ENRICHMENTSK800980HEXTOEN ENTERIC AGARK800979MUELLER HINTIN AGAR W/5% SHEEP BLOOD

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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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