Technicon RA-100(TM) System

FDA 510(k) K883209 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK883209

Submission

Device name
Technicon RA-100(TM) System
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
July 29, 1988
Decision date
September 13, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JJE – Analyzer, Chemistry (Photometric, Discrete), For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2160
Specialty
Clinical Chemistry

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K912616Technicon Immuno 1 TM System Additional AnalytesKLI · Traditional 09/25/1991SE
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K903305Technicon Chem I System Carbon Dioxide MethodKHS · Traditional 09/27/1990SE
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Questions and answers

When was Technicon RA-100(TM) System cleared by the FDA?

Technicon RA-100(TM) System (K883209) received a 510(k) decision of Substantially Equivalent on September 13, 1988, 46 days after the submission was received.

What is the product code of K883209?

The FDA product code is JJE – Analyzer, Chemistry (Photometric, Discrete), For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2160.