Becton Dickinson Thyroid Stimulating Hormone Syste

FDA 510(k) K925132 · Becton Dickinson Advanced Diagnostics

Substantially Equivalent

510(k) numberK925132

Submission

Device name
Becton Dickinson Thyroid Stimulating Hormone Syste
Applicant
Becton Dickinson Advanced Diagnostics
Sparks, MD, US
Received
October 13, 1992
Decision date
December 28, 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 Becton Dickinson Thyroid Stimulating Hormone Syste cleared by the FDA?

Becton Dickinson Thyroid Stimulating Hormone Syste (K925132) received a 510(k) decision of Substantially Equivalent on December 28, 1992, 76 days after the submission was received.

What is the product code of K925132?

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