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FDA 510(k)

THAYER MARTIN AGAR & MODIFIED THAYER AGAR

K-Number: K851587 · 1985-04-30

ApplicantPreferred Micro-Media
Decision Date1985-04-30
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THAYER MARTIN AGAR & MODIFIED THAYER AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Preferred Micro-Media. It received FDA 510(k) clearance on 1985-04-30 under 510(k) number K851587. 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 THAYER MARTIN AGAR & MODIFIED THAYER AGAR?

THAYER MARTIN AGAR & MODIFIED THAYER AGAR is a medical device that received FDA 510(k) clearance on 1985-04-30. The listed applicant is Preferred Micro-Media. The 510(k) number is K851587.

When did THAYER MARTIN AGAR & MODIFIED THAYER AGAR receive FDA 510(k) clearance?

THAYER MARTIN AGAR & MODIFIED THAYER AGAR received FDA 510(k) clearance on 1985-04-30, under 510(k) number K851587.

Who is the listed applicant for THAYER MARTIN AGAR & MODIFIED THAYER AGAR?

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

What is the FDA product code for THAYER MARTIN AGAR & MODIFIED THAYER AGAR?

The FDA product code for THAYER MARTIN AGAR & MODIFIED THAYER AGAR is JTY.

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Other records listing Preferred Micro-Media 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.

K851594SF BROTHK851595SIMMONS CITRATE AGARK851597TRIPLE SUGAR IRON AGARK851593SELECTIVE STREPTOCOCCUS AGARK851592SABOURAUD DEXTROSE AGARK851596SIM MEDIUM

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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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