510(k) K864877

Device
Tri-level Ligand Control
Applicant
CIBA CORNING DIAGNOSTICS CORP.
510(k) number
K864877
Product code
DHX
Decision
Substantially Equivalent (SESE)
Decision date
1987-05-21
Date received
1986-12-12
Regulation
866.6010
Classification name
System, Test, Carcinoembryonic Antigen
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
SCHAEFER, PHD
Address
333 Coney St. East Walpole MA US 02032 02032

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DHX#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K081615OLYMPUS CEA - CARCINOEMBRYONIC ANTIGENOlympus America, Inc.2009-03-18
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K041322VITROS IMMUNODIAGNOSTIC PRODUCTS CEA REAGENT PACK/CALIBRATOR/RANGE VERIFIERSOrtho-Clinical Diagnostics, Inc.2004-06-17
K031270ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY SYSTEMSBeckman Coulter, Inc.2003-05-06
K023893ST AIA-PACK CEA ENZYME IMMUNOASSAYTosoh Medics, Inc.2002-12-18
K013568CEA ASSAY FOR THE ADVIA INTEGRATED MODULAR SYSTEMBayer Corp.2001-12-21
K991707MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206Beckman1999-06-01
K990943VITROS IMMUNODIAGNOSTIC PRODUCTS CEA CALIBRATORS, VITROS IMMUNODIAGNOSTIC PRODUCTS CEA REAGENT PACKOrtho-Clinical Diagnostics, Inc.1999-06-01
K990774ABBOTT ARCHITECT CEAAbbott Laboratories1999-05-11
K981985ACCESS CEA REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL 33200, 33205, 33206 & 33209Beckman Coulter, Inc.1998-09-24
K981478ACS:CENTAUR CEAChiron Diagnostics Corp.1998-08-12