Enzymun Test(R) Tsh-S

FDA 510(k) K900277 · Boehringer Mannheim Corp.

Substantially Equivalent

510(k) numberK900277

Submission

Device name
Enzymun Test(R) Tsh-S
Applicant
Boehringer Mannheim Corp.
Indianapolis, IN, US
Received
January 19, 1990
Decision date
April 11, 1990
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 Enzymun Test(R) Tsh-S cleared by the FDA?

Enzymun Test(R) Tsh-S (K900277) received a 510(k) decision of Substantially Equivalent on April 11, 1990, 82 days after the submission was received.

What is the product code of K900277?

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