THYRODOT-4, THYRODOT-SH
K-Number: K771377 · 1977-09-02
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Device Summary
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
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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