T3 RIA TEST SYSTEM
K-Number: K771220 · 1977-08-04
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Device Summary
Frequently Asked Questions
What is the T3 RIA TEST SYSTEM?
T3 RIA TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1977-08-04. The listed applicant is Monobind. The 510(k) number is K771220.
When did T3 RIA TEST SYSTEM receive FDA 510(k) clearance?
T3 RIA TEST SYSTEM received FDA 510(k) clearance on 1977-08-04, under 510(k) number K771220.
Who is the listed applicant for T3 RIA TEST SYSTEM?
The FDA 510(k) record lists Monobind as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for T3 RIA TEST SYSTEM?
The FDA product code for T3 RIA TEST SYSTEM is CDP.
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 Monobind 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: CDP)
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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