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FDA 510(k)

MARTIN-LEWIS MEDIUM

K-Number: K782117 · 1979-02-01

ApplicantPrepared Media Laboratory, Inc.
Decision Date1979-02-01
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN-LEWIS MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Prepared Media Laboratory, Inc.. It received FDA 510(k) clearance on 1979-02-01 under 510(k) number K782117. 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 MARTIN-LEWIS MEDIUM?

MARTIN-LEWIS MEDIUM is a medical device that received FDA 510(k) clearance on 1979-02-01. The listed applicant is Prepared Media Laboratory, Inc.. The 510(k) number is K782117.

When did MARTIN-LEWIS MEDIUM receive FDA 510(k) clearance?

MARTIN-LEWIS MEDIUM received FDA 510(k) clearance on 1979-02-01, under 510(k) number K782117.

Who is the listed applicant for MARTIN-LEWIS MEDIUM?

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

What is the FDA product code for MARTIN-LEWIS MEDIUM?

The FDA product code for MARTIN-LEWIS MEDIUM 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 Prepared Media Laboratory, 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.

K962744HAEMOPHILUS TEST MEDIUM AGAR (HTM)K962745ENTERIC PATHOGEN TRANSPORT (EPT) (E1020,E1000)

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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