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FDA 510(k)

TRANSGROW

K-Number: K791554 · 1979-09-17

ApplicantAmerican Laboratory Supply, Inc.
Decision Date1979-09-17
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

TRANSGROW is the device name listed in this FDA 510(k) record. The listed applicant is American Laboratory Supply, Inc.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791554. 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?

TRANSGROW is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is American Laboratory Supply, Inc.. The 510(k) number is K791554.

When did TRANSGROW receive FDA 510(k) clearance?

TRANSGROW received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791554.

Who is the listed applicant for TRANSGROW?

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

What is the FDA product code for TRANSGROW?

The FDA product code for TRANSGROW is JTY.

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Other records listing American Laboratory Supply, 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.

K852578CLED AGARK844929INHIBITORY MOLD AGARK844930BRILLANT GREEN AGARK844931MYCOLOGICAL AGAR W/ANTIBIOTICSK844933BILE ESCULIN AGARK844932MALT 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.

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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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