510(k) K032254

Device
IBL C1Q-CIC CIA TEST
Applicant
Ibl GmbH
510(k) number
K032254
Product code
DAK
Decision
Substantially Equivalent (SESE)
Decision date
2003-08-29
Date received
2003-07-22
Regulation
866.5240
Classification name
Complement C1q, Antigen, Antiserum, Control
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
Gary Lehnus
Address
150 Cherry Ln. Rd. East Stroudsburg PA US 18301 18301

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DAK#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K031563BINDAZYME CLQ CIC EIA KITThe Binding Site, Ltd.2003-09-10
K012576CIC-C1Q EIAAmerican Laboratory Products Co., Ltd.2002-01-29
K973203THYMOSTAT ELISA FOR THE DETECTION OF HUMAN IGG,M AND A ANTI-RABBIT IGG ANTIBODIESSangstat Medical Corp.1998-09-30
K972873IMMUSTRIP HAMA IGGImmunomedics, Inc.1998-03-17
K951968HUMAN C1Q RADIAL IMMUNODIFFUSION KITKent Laboratories, Inc.1995-05-30
K914388C1 RID KITThe Binding Site, Ltd.1991-10-28
K882829CIRCULATING IMMUNE COMPLEXES CONTROLSCytotech, Inc.1988-08-04
K860996SANASSAY IC TESTScientific Sales Intl., Inc.1987-03-30
K864312IC MICROASSAYDiamedix Corp.1987-01-09
K862649CYTOTECH CIC ENZYME IMMUNOASSAYCytotech, Inc.1986-09-04
K861499BIOSTAR* READS* IMMUNE COMPLEX ASSAY KITBiostar Medical Products, Inc.1986-06-20
K853697BIOSTAR RE-A-DS IMMUNE COMPLEX ASSAY KITBiostar Medical Products, Inc.1985-12-16
K851202GILFORD TRI-LEVEL ASSAYED IMMUNOLOGY CONTROLGilford1985-04-29
K844294CORDIA ICCordis Corp.1985-02-04
K833275GMP CIQ ELISA TEST KITGamma Medical Products, Inc.1984-06-22