Radias Neonatal TSH Enzyme Immunoassay

FDA 510(k) K935399 · Bio-Rad

Substantially Equivalent

510(k) numberK935399

Submission

Device name
Radias Neonatal TSH Enzyme Immunoassay
Applicant
Bio-Rad
Hercules, CA, US
Received
November 9, 1993
Decision date
December 19, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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 Radias Neonatal TSH Enzyme Immunoassay cleared by the FDA?

Radias Neonatal TSH Enzyme Immunoassay (K935399) received a 510(k) decision of Substantially Equivalent on December 19, 1994, 405 days after the submission was received.

What is the product code of K935399?

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