Ultrasensitive TSH (U-Tsh) Enzyme Immuno Test Kit

FDA 510(k) K914756 · Medix Biotech, Inc.

Substantially Equivalent

510(k) numberK914756

Submission

Device name
Ultrasensitive TSH (U-Tsh) Enzyme Immuno Test Kit
Applicant
Medix Biotech, Inc.
Foster City, CA, US
Received
October 22, 1991
Decision date
January 15, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
JLW – Radioimmunoassay, Thyroid-Stimulating Hormone
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1690
Specialty
Clinical Chemistry

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Questions and answers

When was Ultrasensitive TSH (U-Tsh) Enzyme Immuno Test Kit cleared by the FDA?

Ultrasensitive TSH (U-Tsh) Enzyme Immuno Test Kit (K914756) received a 510(k) decision of Substantially Equivalent on January 15, 1992, 85 days after the submission was received.

What is the product code of K914756?

The FDA product code is JLW – Radioimmunoassay, Thyroid-Stimulating Hormone, a Class II (moderate risk) device regulated under 21 CFR 862.1690.