Synchron Systems Thyroxine Reagent

FDA 510(k) K971203 · Beckman Instruments, Inc.

Substantially Equivalent

510(k) numberK971203

Submission

Device name
Synchron Systems Thyroxine Reagent
Applicant
Beckman Instruments, Inc.
Brea, CA, US
Received
April 1, 1997
Decision date
May 16, 1997
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1700
Specialty
Clinical Chemistry

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Questions and answers

When was Synchron Systems Thyroxine Reagent cleared by the FDA?

Synchron Systems Thyroxine Reagent (K971203) received a 510(k) decision of Substantially Equivalent on May 16, 1997, 45 days after the submission was received.

What is the product code of K971203?

The FDA product code is KLI – Enzyme Immunoassay, Non-Radiolabeled, Total Thyroxine, a Class II (moderate risk) device regulated under 21 CFR 862.1700.