Technicon Star System T3 Ria Method

FDA 510(k) K810798 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK810798

Submission

Device name
Technicon Star System T3 Ria Method
Applicant
Technicon Instruments Corp.
Mchenry, IL, US
Received
March 23, 1981
Decision date
April 7, 1981
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDP – Radioimmunoassay, Total Triiodothyronine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1710
Specialty
Clinical Chemistry

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K974634Immulite Free T3CDP · Traditional Diagnostic Products Corp.01/02/1998SE
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Questions and answers

When was Technicon Star System T3 Ria Method cleared by the FDA?

Technicon Star System T3 Ria Method (K810798) received a 510(k) decision of Substantially Equivalent on April 7, 1981, 15 days after the submission was received.

What is the product code of K810798?

The FDA product code is CDP – Radioimmunoassay, Total Triiodothyronine, a Class II (moderate risk) device regulated under 21 CFR 862.1710.