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FDA 510(k)

MARTIN-LEWIS/PRONG AGAR

K-Number: K821551 · 1982-06-22

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1982-06-22
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN-LEWIS/PRONG AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1982-06-22 under 510(k) number K821551. 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/PRONG AGAR?

MARTIN-LEWIS/PRONG AGAR is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K821551.

When did MARTIN-LEWIS/PRONG AGAR receive FDA 510(k) clearance?

MARTIN-LEWIS/PRONG AGAR received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821551.

Who is the listed applicant for MARTIN-LEWIS/PRONG AGAR?

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

What is the FDA product code for MARTIN-LEWIS/PRONG AGAR?

The FDA product code for MARTIN-LEWIS/PRONG AGAR is JTY.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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K871855SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORMK871541MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226K870134MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PREK864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORMK864014LOMBARD DOWELL AGAR BASEK863821MUELLER HINTON AGAR W/4%NACL AND OXACILLIN

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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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