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Scimedx Corp.

14 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
PHASE II GBM IGG ANTIBODY EIA TEST (K011348)Scimedx Corp.2001-06-25
TPO IGG ANTIBODY EIA TEST (K011082)Scimedx Corp.2001-06-06
EUROSPITAL EU-TTG IGA UMANA (K010625)Scimedx Corp.2001-04-24
SCIMEDX PHASE II PR3 IGG ANTIBODY EIA (K010287)Scimedx Corp.2001-03-16
SCIMEDX PHASE II MPO IGG ANTIBODY EIA (K010289)Scimedx Corp.2001-03-07
GLIADIN IGA ANTIBODY EIA DETECTION SYSTEM (K002169)Scimedx Corp.2000-10-19
GLIADIN IGG ANTIBODY EIA DETECTION SYSTEM (K002189)Scimedx Corp.2000-10-19
IFA KIT FOR THE DETECTION OF ENDOMYSIAL IGA ANIBODIES USING PRIMATE UMBILICAL CORD (PUC)-EMA/PUC LGA. (K002107)Scimedx Corp.2000-08-04
EU-TTG IGA ELISA (K994379)Scimedx Corp.2000-02-18
IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES (K970198)Scimedx Corp.1997-02-20
IFA KIT FOR THE DETECTION OF C-ANCA ANTIBODIES (K962360)Scimedx Corp.1996-09-30
EIA KIT FOR THE DETECTION OF GBM ANTIBODIES (K953495)Scimedx Corp.1996-04-10
EIA KIT FOR THE DETCTION OF ANTI-PR3 ANTIBODIES (K954105)Scimedx Corp.1996-03-19
EIA KIT FOR THE DETECTION OF ANTI-MPO ANTIBODIES (K954062)Scimedx Corp.1996-03-19

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Every clearance here is in the API, with alerts when new ones post.