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FDA 510(k)

IMPROVED THAYER MARTIN (PLATE)

K-Number: K770874 · 1977-06-08

ApplicantGranite Diagnostics, Inc.
Decision Date1977-06-08
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IMPROVED THAYER MARTIN (PLATE) is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-06-08 under 510(k) number K770874. 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 IMPROVED THAYER MARTIN (PLATE)?

IMPROVED THAYER MARTIN (PLATE) is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K770874.

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

IMPROVED THAYER MARTIN (PLATE) received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770874.

Who is the listed applicant for IMPROVED THAYER MARTIN (PLATE)?

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

What is the FDA product code for IMPROVED THAYER MARTIN (PLATE)?

The FDA product code for IMPROVED THAYER MARTIN (PLATE) is JTY.

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Other records listing Granite Diagnostics, Inc. as applicant

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K850969INHIBITORY MOLD AGAR PLATEK850970BRAIN HEART INFUSION AGAR W/5% SHEEP BLOOD, CHLORAK833254STREPTOCOCCUS ID TRIPLATE SYSTEMK832365TCBS AGARK831349STREPTOCOCUS ID PLATEK830252DIPCHEX DIP-SLIDE CULTURE SYS

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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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