FDA.reportPublic FDA data

510(k) K834605

Device
C4 Antigen Antibody Control
Applicant
TECHNICON INSTRUMENTS CORP.
510(k) number
K834605
Product code
DBI
Decision
Substantially Equivalent (SESE)
Decision date
1984-01-24
Date received
1983-09-30
Regulation
866.5240
Classification name
Complement C4, Antigen, Antiserum, Control
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DBI#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K100455SPAPLUS ANALYZERThe Binding Site2010-09-03
K012359TINA-QUANT COMPLEMENT C4 TEST SYSTEMRoche Diagnostics Corp.2001-11-29
K010325WAKO AUTOKIT C4Wako Chemicals USA, Inc.2001-06-25
K000468RANDOX COMPLEMENT C4Randox Laboratories, Ltd.2000-03-27
K994293DIMENSION C4 FLEX REAGENT CARTRIDGEDade Behring, Inc.2000-03-01
K981785C4 MININEPH ANTISERUMThe Binding Site, Ltd.1999-12-20
K993481K-ASSAY C4Kamiya Biomedical Co.1999-11-29
K983356C4Abbott Laboratories1998-11-04
K964300N-ASSAY TIA MULTI V-NLCrestat Diagnostics, Inc.1997-07-14
K964297N-ASSAY TIA C4 TEST KITCrestat Diagnostics, Inc.1997-07-14
K962582OLYMPUS C4 IMMUNOTURBIDIMETRIC REAGENTOlympus America, Inc.1996-10-18
K962198QUANTEX C4Instrumentation Laboratory CO1996-09-26
K920010IL TEST COMPLEMENT 4Instrumentation Laboratory CO1992-03-13
K911899RAICHEM SPIA C4 REAGENTReagents Applications, Inc.1991-05-09
K892129EZ COMPLEMENT C4Diamedix Corp.1989-04-14