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FDA 510(k)

IMPROVED THAYER MARTIN MEDIUM

K-Number: K760598 · 1976-10-08

ApplicantScott Laboratories, Inc.
Decision Date1976-10-08
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IMPROVED THAYER MARTIN MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Scott Laboratories, Inc.. It received FDA 510(k) clearance on 1976-10-08 under 510(k) number K760598. 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 MEDIUM?

IMPROVED THAYER MARTIN MEDIUM is a medical device that received FDA 510(k) clearance on 1976-10-08. The listed applicant is Scott Laboratories, Inc.. The 510(k) number is K760598.

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

IMPROVED THAYER MARTIN MEDIUM received FDA 510(k) clearance on 1976-10-08, under 510(k) number K760598.

Who is the listed applicant for IMPROVED THAYER MARTIN MEDIUM?

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

What is the FDA product code for IMPROVED THAYER MARTIN MEDIUM?

The FDA product code for IMPROVED THAYER MARTIN MEDIUM is JTY.

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Other records listing Scott Laboratories, Inc. as applicant

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K880694B. CAT CONFIRMK874933MUG-INDOLE DISCK874662MYCO-FLUOR REAGENT A & BK873509IDENTICULT-BLK871238ANABAGK863025SERO-STAT R II STAPHYLOCOCCUS TEST

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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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