Testosterone Coated Tubes Radioimmunoassay Kit

FDA 510(k) K860130 · Cambridge Medical Technology

Substantially Equivalent

510(k) numberK860130

Submission

Device name
Testosterone Coated Tubes Radioimmunoassay Kit
Applicant
Cambridge Medical Technology
Billerica, MA, US
Received
January 14, 1986
Decision date
February 19, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CDZ – Radioimmunoassay, Testosterones And Dihydrotestosterone
Device class
Class I (low risk)
Regulation
21 CFR 862.1680
Specialty
Clinical Chemistry

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K873737No Spin(Tm) T3 Coated Tube RadioimmunoassayCDP · Traditional 11/24/1987SE
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K855169T3 Uptake Radioimmunoassay KitKHQ · Traditional 02/06/1986SE
K850254Parathyroid Hormone Radioimmunoassay KitCEW · Traditional 04/03/1985SE
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Questions and answers

When was Testosterone Coated Tubes Radioimmunoassay Kit cleared by the FDA?

Testosterone Coated Tubes Radioimmunoassay Kit (K860130) received a 510(k) decision of Substantially Equivalent on February 19, 1986, 36 days after the submission was received.

What is the product code of K860130?

The FDA product code is CDZ – Radioimmunoassay, Testosterones And Dihydrotestosterone, a Class I (low risk) device regulated under 21 CFR 862.1680.