Technicon Chem 1(TM) System

FDA 510(k) K874916 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK874916

Submission

Device name
Technicon Chem 1(TM) System
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
December 3, 1987
Decision date
March 3, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
LDR – Controller, Infusion, Intravascular, Electronic
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5725
Specialty
General Hospital

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More from The Master Medical Corp.

510(k)DeviceDecision
K914888Technicon Chem 1(TM) Syst (GEN2 Syst)CIX · Traditional 11/27/1991SE
K914511Technicon Axon(Tm) System Methods Anyalye HDL CholLBS · Traditional 11/27/1991SE
K914025Technicon Axon(Tm) Systems, Alt(P 5-P)/AST(P 5-P)CIT · Traditional 11/22/1991SE
K912616Technicon Immuno 1 TM System Additional AnalytesKLI · Traditional 09/25/1991SE
K912413Chem-Link Data Base ManagerJJQ · Traditional 07/01/1991SE
K903825Drug of Abuse Analysis SystemDIS · Traditional 09/27/1990SE
K903824Drug of Abuse Analysis System Free Radical AssayDKZ · Traditional 09/27/1990SE
K903305Technicon Chem I System Carbon Dioxide MethodKHS · Traditional 09/27/1990SE
K903306Technicon Chem I System Magnesium MethodJGJ · Traditional 08/29/1990SE
K901410Technicon RA-2000(TM) SystemJJC · Traditional 07/17/1990SE

Questions and answers

When was Technicon Chem 1(TM) System cleared by the FDA?

Technicon Chem 1(TM) System (K874916) received a 510(k) decision of Substantially Equivalent on March 3, 1988, 91 days after the submission was received.

What is the product code of K874916?

The FDA product code is LDR – Controller, Infusion, Intravascular, Electronic, a Class II (moderate risk) device regulated under 21 CFR 880.5725.