Cooper Biomedical, Inc.
Cooper Biomedical, Inc. holds FDA 510(k) medical device clearances, first cleared 1983, most recent 1987.
Top product codes for Cooper Biomedical, Inc.
Recent clearances by Cooper Biomedical, Inc.
- K863868 — IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/ALPHA-1 ANT
- K864512 — IMMUNO-PLATE IV RADIAL IMMUNO TEST KIT/HUMAN HAPTO
- K863301 — DEMAND TOTAL PROTEIN
- K861926 — WORTHINGTON HDL PRECIPITATING REAGENT SET
- K854130 — DEMAND ETHYL ALCOHOL
- K853949 — DEMAND ACID PHOSPHATASE REAGENT
- K852262 — ASSIST CLINICAL CHEMISTRY ANALYZER
- K851285 — RADIAL IMMUNODIFFUSION PLATES CSF IGG & CSF ALBUMI
- K851284 — RADIAL IMMUNO-DIFFUSION PLATES IGA, IGD, IGG & IGM
- K851286 — RADIAL IMMUNODIFFUSION PLATES C3 & C4
- K851282 — RADIAL IMMUNODIFFUSION PLATES ALPHA-2 MACROGLOBULI
- K851287 — RADIAL IMMUNODIFFUSION PLATES TRANSFERRIN
- K851283 — RADIAL IMMUNODIFFUSION PLATES-CERULOPLASMIN
- K851657 — DEMAND MAGNESIUM
- K842484 — LEAP LE TEST KIT
- K841726 — DEMAND C02
- K841076 — ION SELECTIVE ELECTRODE
- K840822 — LEAP MONO TEST KIT
- K833738 — LEAP STREP TEST KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.