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FDA 510(k)

TRANSGROW MEDIUM

K-Number: K832862 · 1983-09-26

ApplicantTroy Biologicals, Inc.
Decision Date1983-09-26
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRANSGROW MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Troy Biologicals, Inc.. It received FDA 510(k) clearance on 1983-09-26 under 510(k) number K832862. 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 TRANSGROW MEDIUM?

TRANSGROW MEDIUM is a medical device that received FDA 510(k) clearance on 1983-09-26. The listed applicant is Troy Biologicals, Inc.. The 510(k) number is K832862.

When did TRANSGROW MEDIUM receive FDA 510(k) clearance?

TRANSGROW MEDIUM received FDA 510(k) clearance on 1983-09-26, under 510(k) number K832862.

Who is the listed applicant for TRANSGROW MEDIUM?

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

What is the FDA product code for TRANSGROW MEDIUM?

The FDA product code for TRANSGROW MEDIUM is JTY.

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Other records listing Troy Biologicals, 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.

K861301BACTI PLATE (DERMATOLOGY) PRODUCT NO. PS-5000K832860SXT BLOOD AGARK832863STREP ID QUADK832861SABOURAUD DEXTROSE AGARK823307CAMPYLOBACTER SELECTIVE AGARK823311COLUMBIA V AGAR W/5% HUMAN BLOOD

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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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