CLINIRIA TOTAL T-4 (RIA) TEST
K-Number: K781181 · 1978-08-14
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Device Summary
Frequently Asked Questions
What is the CLINIRIA TOTAL T-4 (RIA) TEST?
CLINIRIA TOTAL T-4 (RIA) TEST is a medical device that received FDA 510(k) clearance on 1978-08-14. The listed applicant is Miles Laboratories, Inc.. The 510(k) number is K781181.
When did CLINIRIA TOTAL T-4 (RIA) TEST receive FDA 510(k) clearance?
CLINIRIA TOTAL T-4 (RIA) TEST received FDA 510(k) clearance on 1978-08-14, under 510(k) number K781181.
Who is the listed applicant for CLINIRIA TOTAL T-4 (RIA) TEST?
The FDA 510(k) record lists Miles Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLINIRIA TOTAL T-4 (RIA) TEST?
The FDA product code for CLINIRIA TOTAL T-4 (RIA) TEST is CDX.
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 Miles Laboratories, 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: CDX)
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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