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FDA 510(k)

IMPROVED THAYER-MARTIN MEDIUM

K-Number: K770925 · 1977-06-08

Decision Date1977-06-08
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

IMPROVED THAYER-MARTIN MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Tech Diagnostic, Inc.. It received FDA 510(k) clearance on 1977-06-08 under 510(k) number K770925. 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 IMPROVED THAYER-MARTIN MEDIUM?

IMPROVED THAYER-MARTIN MEDIUM is a medical device that received FDA 510(k) clearance on 1977-06-08. The listed applicant is Micro-Tech Diagnostic, Inc.. The 510(k) number is K770925.

When did IMPROVED THAYER-MARTIN MEDIUM receive FDA 510(k) clearance?

IMPROVED THAYER-MARTIN MEDIUM received FDA 510(k) clearance on 1977-06-08, under 510(k) number K770925.

Who is the listed applicant for IMPROVED THAYER-MARTIN MEDIUM?

The FDA 510(k) record lists Micro-Tech Diagnostic, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPROVED THAYER-MARTIN MEDIUM?

The FDA product code for IMPROVED THAYER-MARTIN MEDIUM is JTY.

Related Clinical Trials

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.

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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