Microzyme Thyroid Uptake Enzyme Immunoassay Kit

FDA 510(k) K905777 · Immunotech Corp.

Substantially Equivalent

510(k) numberK905777

Submission

Device name
Microzyme Thyroid Uptake Enzyme Immunoassay Kit
Applicant
Immunotech Corp.
Boston, MA, US
Received
December 27, 1990
Decision date
January 30, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CEE – Radioimmunoassay, Thyroxine-Binding Globulin
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1685
Specialty
Clinical Chemistry

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K874658Technicon Ra(R) Analyte (TBG) (30 C and 37 C)CEE · Traditional Technicon Instruments Corp.12/18/1987SE
K862109Enzymun Test TBGCEE · Traditional Boehringer Mannheim Corp.06/30/1986SE

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Questions and answers

When was Microzyme Thyroid Uptake Enzyme Immunoassay Kit cleared by the FDA?

Microzyme Thyroid Uptake Enzyme Immunoassay Kit (K905777) received a 510(k) decision of Substantially Equivalent on January 30, 1991, 34 days after the submission was received.

What is the product code of K905777?

The FDA product code is CEE – Radioimmunoassay, Thyroxine-Binding Globulin, a Class II (moderate risk) device regulated under 21 CFR 862.1685.