TRI-TAB-RIA
K-Number: K772177 · 1977-12-22
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Device Summary
Frequently Asked Questions
What is the TRI-TAB-RIA?
TRI-TAB-RIA is a medical device that received FDA 510(k) clearance on 1977-12-22. The listed applicant is Nuclear Medical Laboratories, Inc.. The 510(k) number is K772177.
When did TRI-TAB-RIA receive FDA 510(k) clearance?
TRI-TAB-RIA received FDA 510(k) clearance on 1977-12-22, under 510(k) number K772177.
Who is the listed applicant for TRI-TAB-RIA?
The FDA 510(k) record lists Nuclear Medical Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRI-TAB-RIA?
The FDA product code for TRI-TAB-RIA is CDP.
Other records listing Nuclear Medical 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: 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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