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FDA 510(k)

THAYER MARTIN AGAR

K-Number: K833862 · 1983-12-12

ApplicantAmerican Biomedical Corp.
Decision Date1983-12-12
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 American Biomedical Corp.. It received FDA 510(k) clearance on 1983-12-12 under 510(k) number K833862. 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 1983-12-12. The listed applicant is American Biomedical Corp.. The 510(k) number is K833862.

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

THAYER MARTIN AGAR received FDA 510(k) clearance on 1983-12-12, under 510(k) number K833862.

Who is the listed applicant for THAYER MARTIN AGAR?

The FDA 510(k) record lists American Biomedical Corp. 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.

Related Clinical Trials

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.

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Other records listing American Biomedical Corp. 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.

K833861MUELLER HINTON AGAR

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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