TSH Maiaclone Immunoradiometric Assay Kit/Mag Sep

FDA 510(k) K864677 · Serono Diagnostics, Inc.

Substantially Equivalent

510(k) numberK864677

Submission

Device name
TSH Maiaclone Immunoradiometric Assay Kit/Mag Sep
Applicant
Serono Diagnostics, Inc.
Norwell, MA, US
Received
December 2, 1986
Decision date
January 7, 1987
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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 TSH Maiaclone Immunoradiometric Assay Kit/Mag Sep cleared by the FDA?

TSH Maiaclone Immunoradiometric Assay Kit/Mag Sep (K864677) received a 510(k) decision of Substantially Equivalent on January 7, 1987, 36 days after the submission was received.

What is the product code of K864677?

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