Chem-Link Data Base Manager

FDA 510(k) K912413 · Technicon Instruments Corp.

Substantially Equivalent

510(k) numberK912413

Submission

Device name
Chem-Link Data Base Manager
Applicant
Technicon Instruments Corp.
Tarrytown, NY, US
Received
May 31, 1991
Decision date
July 1, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use
Device class
Class I (low risk)
Regulation
21 CFR 862.2300
Specialty
Clinical Chemistry

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K973938Alpha 4 LS Automated Microtiterplate Processor and ReaderJJQ · Traditional Sfri, Inc.02/04/1998SE
K974762Stat TracksJJQ · Traditional Awareness Technology, Inc.01/28/1998SE
K962113Anthos Phacts Version Microplate ReaderJJQ · Traditional Columbia Bioscience, Inc.11/05/1996SE
K961183Cbi 7520 ReaderJJQ · Traditional Columbia Bioscience, Inc.08/02/1996SE
K962166Origen AnalyzerJJQ · Traditional Igen, Inc.07/31/1996SE
K955077Anthos 2010 ReaderJJQ · Traditional Anthos Labtec, Inc.12/04/1995SE
K953710ELX808 Automated Microplate ReadersJJQ · Traditional Bio-Tek Instruments, Inc.10/25/1995SE
K953572ELX800UVJJQ · Traditional Bio-Tek Instruments, Inc.10/19/1995SE

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K912616Technicon Immuno 1 TM System Additional AnalytesKLI · Traditional 09/25/1991SE
K903825Drug of Abuse Analysis SystemDIS · Traditional 09/27/1990SE
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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
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Questions and answers

When was Chem-Link Data Base Manager cleared by the FDA?

Chem-Link Data Base Manager (K912413) received a 510(k) decision of Substantially Equivalent on July 1, 1991, 31 days after the submission was received.

What is the product code of K912413?

The FDA product code is JJQ – Colorimeter, Photometer, Spectrophotometer For Clinical Use, a Class I (low risk) device regulated under 21 CFR 862.2300.