Scimedx Corp.
FDA 510(k) medical device clearances.
Top product codes for Scimedx Corp.
Recent clearances by Scimedx Corp.
- K011348 — PHASE II GBM IGG ANTIBODY EIA TEST
- K011082 — TPO IGG ANTIBODY EIA TEST
- K010625 — EUROSPITAL EU-TTG IGA UMANA
- K010287 — SCIMEDX PHASE II PR3 IGG ANTIBODY EIA
- K010289 — SCIMEDX PHASE II MPO IGG ANTIBODY EIA
- K002169 — GLIADIN IGA ANTIBODY EIA DETECTION SYSTEM
- K002189 — GLIADIN IGG ANTIBODY EIA DETECTION SYSTEM
- K002107 — IFA KIT FOR THE DETECTION OF ENDOMYSIAL IGA ANIBODIES USING PRIMATE UMBILICAL CORD (PUC)-EMA/PUC LGA.
- K994379 — EU-TTG IGA ELISA
- K970198 — IFA HEP2 KIT FOR THE DETECTION OF ANTINUCLEAR ANTIBODIES
- K962360 — IFA KIT FOR THE DETECTION OF C-ANCA ANTIBODIES
- K953495 — EIA KIT FOR THE DETECTION OF GBM ANTIBODIES
- K954062 — EIA KIT FOR THE DETECTION OF ANTI-MPO ANTIBODIES
- K954105 — EIA KIT FOR THE DETCTION OF ANTI-PR3 ANTIBODIES
Data sourced from openFDA. This site is unofficial and independent of the FDA.