TRIA-PEG RIA DIAG. KIT
K-Number: K780292 · 1978-03-02
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Device Summary
Frequently Asked Questions
What is the TRIA-PEG RIA DIAG. KIT?
TRIA-PEG RIA DIAG. KIT is a medical device that received FDA 510(k) clearance on 1978-03-02. The listed applicant is Nuclear Diagnostics, Inc.. The 510(k) number is K780292.
When did TRIA-PEG RIA DIAG. KIT receive FDA 510(k) clearance?
TRIA-PEG RIA DIAG. KIT received FDA 510(k) clearance on 1978-03-02, under 510(k) number K780292.
Who is the listed applicant for TRIA-PEG RIA DIAG. KIT?
The FDA 510(k) record lists Nuclear Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRIA-PEG RIA DIAG. KIT?
The FDA product code for TRIA-PEG RIA DIAG. KIT is CDP.
Other records listing Nuclear 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: 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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