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FDA 510(k)

THYRODOT-4, THYRODOT-SH

K-Number: K771377 · 1977-09-02

Decision Date1977-09-02
Product CodeJLW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

THYRODOT-4, THYRODOT-SH is the device name listed in this FDA 510(k) record. The listed applicant is Medcom Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-09-02 under 510(k) number K771377. The device is classified under product code JLW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THYRODOT-4, THYRODOT-SH?

THYRODOT-4, THYRODOT-SH is a medical device that received FDA 510(k) clearance on 1977-09-02. The listed applicant is Medcom Diagnostics, Inc.. The 510(k) number is K771377.

When did THYRODOT-4, THYRODOT-SH receive FDA 510(k) clearance?

THYRODOT-4, THYRODOT-SH received FDA 510(k) clearance on 1977-09-02, under 510(k) number K771377.

Who is the listed applicant for THYRODOT-4, THYRODOT-SH?

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

What is the FDA product code for THYRODOT-4, THYRODOT-SH?

The FDA product code for THYRODOT-4, THYRODOT-SH is JLW.

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.

Other records listing Medcom Diagnostics, 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.

Related Devices (Code: JLW)

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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