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FDA 510(k)

MOD THAYER MARTIN MARTIN LEWIS

K-Number: K850841 · 1985-03-20

ApplicantMicro Media Laboratories
Decision Date1985-03-20
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MOD THAYER MARTIN MARTIN LEWIS is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850841. 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 MOD THAYER MARTIN MARTIN LEWIS?

MOD THAYER MARTIN MARTIN LEWIS is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Micro Media Laboratories. The 510(k) number is K850841.

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

MOD THAYER MARTIN MARTIN LEWIS received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850841.

Who is the listed applicant for MOD THAYER MARTIN MARTIN LEWIS?

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

What is the FDA product code for MOD THAYER MARTIN MARTIN LEWIS?

The FDA product code for MOD THAYER MARTIN MARTIN LEWIS is JTY.

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Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGARK853691TERGITOL 7 AGARK851344OXIDATIVE FORMENTIVE MEDIUMK851345PURPLE BROTHK851343BROM CRESOL PURPLE STARCHK851348COBA 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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