Synchron CX4-CE

FDA 510(k) K904220 · Beckman

Substantially Equivalent

510(k) numberK904220

Submission

Device name
Synchron CX4-CE
Applicant
Beckman
Brea, CA, US
Received
September 12, 1990
Decision date
October 15, 1990
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

Other 510(k)s with product code JJE

510(k)DeviceApplicantDecision
K183375Yumizen C1200, Yumizen C1200 Glucose HK, Sodium Electrode, Potassium Electrode, Chloride…JJE · Traditional Horiba, Ltd.02/12/2019SE
K133519Carolina Liquid Chemistries CLC 6410 Chemistry Analyzer; Carolina Liquid Chemistries…JJE · Traditional Carolina Liquid Chemistries Corp.05/16/2014SE
K130915XL-200 Clinical Chemistry Analyzer, Jas Glucose Reagent, Ise Reagent PackJJE · Traditional Jas Diagnostics, Inc.05/15/2014SE
K131554RX Daytona Plus Chemistry Analyzer; RX Daytona Plus Aspartate Aminotransferase (Ast)…JJE · Traditional Randox Laboratories, Ltd.01/09/2014SE
K130276Dimension Exl with LM SystemJJE · Traditional Siemens Healthcare Diagnostics, Inc.03/22/2013SE
K113253Ace Axcel Clinical Chemistry System,Ace Albumin Reagent,Ace Total Protein Reagent,Ace…JJE · Traditional Alfa Wassermann Diagnostic Technologies, Inc.05/17/2012SE
K112999Dimension Clinical Chemistry SystemJJE · Special Siemens Healthcare Diagnostics11/22/2011SE
K110035IndikoJJE · Traditional Thermofisher Scientific OY06/28/2011SE
K073370TC Matrix Clinical Chemistry AnalyzerJJE · Traditional Teco Diagnostics05/08/2008SE
K063144Vitros 5,1 FS Chemistry System with Engen Laboratory Automation SystemJJE · Special Ortho-Clinical Diagnostics, Inc.11/13/2006SE

More from Ortho-Clinical Diagnostics, Inc.

510(k)DeviceDecision
K991707Modification to Access Cea Reagents for Use on the Access Immunoassay Analyzer, Models…DHX · Special 06/01/1999SE
K971534Synchron Syustems Dat Drug Free Urine ControlDIF · Traditional 05/21/1997SE
K935362P-Amylase ControlJJX · Traditional 01/27/1994SE
K904219Synchron CX 7 Clinical AnalyzerJJE · Traditional 10/22/1990SE
K893583Beckman Cholinesterase Reagent KitDIH · Traditional 08/15/1989SE

Questions and answers

When was Synchron CX4-CE cleared by the FDA?

Synchron CX4-CE (K904220) received a 510(k) decision of Substantially Equivalent on October 15, 1990, 33 days after the submission was received.

What is the product code of K904220?

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.