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FDA 510(k)

THAYER-MARTIN JEMBEC

K-Number: K864252 · 1987-03-31

ApplicantMds Laboratories, Inc.
Decision Date1987-03-31
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER-MARTIN JEMBEC is the device name listed in this FDA 510(k) record. The listed applicant is Mds Laboratories, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K864252. 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 JEMBEC?

THAYER-MARTIN JEMBEC is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Mds Laboratories, Inc.. The 510(k) number is K864252.

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

THAYER-MARTIN JEMBEC received FDA 510(k) clearance on 1987-03-31, under 510(k) number K864252.

Who is the listed applicant for THAYER-MARTIN JEMBEC?

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

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

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

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Other records listing Mds Laboratories, 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.

K864241DNASE AGARK864242HEKTOEN ENTERIC AGARK864247MUELLER HINTON AGAR WITH 5% SHEEP BLOODK864244GARNERELLA VAGINALIS IDENTIFICATION KITK864249NORMAL SALINE STERILEK864243MACCONKEY 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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