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FDA 510(k)

MARTIN LEWIS TRANSGROW

K-Number: K771872 · 1977-10-25

ApplicantGranite Diagnostics, Inc.
Decision Date1977-10-25
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN LEWIS TRANSGROW is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771872. 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 TRANSGROW?

MARTIN LEWIS TRANSGROW is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K771872.

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

MARTIN LEWIS TRANSGROW received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771872.

Who is the listed applicant for MARTIN LEWIS TRANSGROW?

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

What is the FDA product code for MARTIN LEWIS TRANSGROW?

The FDA product code for MARTIN LEWIS TRANSGROW is JTY.

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Related Devices (Code: JTY)

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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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