Medical Diagnostic Technologies, Inc.
FDA 510(k) medical device clearances.
Top product codes for Medical Diagnostic Technologies, Inc.
Recent clearances by Medical Diagnostic Technologies, Inc.
- K062229 — CTC WORKSTATION, MODEL 2200
- K972209 — SPECTROLYSE HEPARIN (ANTI-IIA)
- K963106 — CHROMOLIZE PAI-1 KIT
- K960871 — SPECTROLYSE ANTITHROMBIN III (ANTI-XA)
- K962489 — CHROMOLIZE TPA ASSAY KIT
- K960438 — TINTELIZE PAI-1 KIT
- K961724 — U-DOA CONTROLS
- K961370 — LA POSITIVE CONTROL PLASMA
- K955115 — VENOM TIEM REAGENT
- K955738 — BIOCLOT PROTEIN S
- K952746 — ALKALINE PHOSPHATASE REAGENT SYSTEM
- K952743 — ASPARTATE AMINOTRANSFERASE REAGENT SYSTEM
- K952741 — TRIGLYCERIDES (GLYCEROL BLANKING) REAGENT SYSTEM
- K952742 — BLOOD UREA NITROGEN REAGENT SYSTEM
- K952745 — CREATINE KINASE REAGENT SYSTEM
- K952744 — ALANINE AMINOTRANSFERASE REAGENT SYSTEM
- K952747 — LACTATE DEHYDROGENASE REAGENT SYSTEM
- K942093 — REMEL RIM STREPTOCOCCUS GROUPING LATEX AGGLUTINATION TEST
- K942257 — DOA-PLUS, DRUGS OF ABUSE CONTROLS
- K940457 — LIPASE REAGENT SYSTEM
- K935285 — DRUGS OF ABUSE CONTROLS
- K934351 — APTT-ES REAGENT
- K921556 — MYCOPLASMA PNEUMONIAE IGG/IGM ANTIBODY TEST SYSTEM
- K920981 — RISTOCETIN COFACTOR ASSAY/VON WILLEBRAND FACT ASSA
- K911145 — BORRELIA BURGDORFERI POLYVAL IGG/IGM ANTIBODY TEST
- K910286 — PLATELET AGGREGATION REAGENTS
- K904501 — MYCOPLASMA PNEUMONIAE ANTIBODY TEST SYSTEM
- K905203 — COAGULATION REFERENCE PLASMA, NORMAL
- K900782 — HEPARIN CONTROL PLASMA, FOR USE IN APTT
- K900792 — RISTOCETIN
- K900049 — APTT-EA REAGENT, AN ELLAGIC ACID ACTIVATED REAGENT
- K900133 — FACTOR II DEFICIENT PLASMA
- K896625 — THROMBOPLASTIN, FOR USE IN PROTHROMBIN TIME DETER.
- K896052 — FIBRINOGEN ASSAY KIT
- K896033 — FDP COLLECTION TUBES
- K895255 — APTT-P REAGENT, A PARTICLE ACTIVATED REAGENT
- K895260 — ABNORMAL COAGULATION CONTROL PLASMA-1 (ACCP-1)
- K895261 — ABNORMAL COAGULATION CONTROL PLASMA-2 (ACCP-2)
- K895262 — NORMAL COAGULATION CONTROL PLASMA (NCCP)
- K895503 — ABNORMAL REFERENCE PLASMA-VIII
- K895504 — ABNORMAL REFERENCE PLASMA-IX
- K893523 — FACTOR X DEFICIENT PLASMA
- K893524 — FACTOR IX DEFICIENT PLASMA
- K893525 — FACTOR VIII DEFICIENT PLASMA
- K893533 — FACTOR V DEFICIENT PLASMA
- K893534 — FACTOR XII DEFICIENT PLASMA
- K893535 — FACTOR VII DEFICIENT PLASMA
- K893536 — FACTOR XI DEFICIENT PLASMA
- K885290 — BORRELIA BURGDORFERI POLYVALENT IGG/IGM ANTIBODY
- K885293 — BORRELIA BURGDORFERI IGG ANTIBODY TEST SYSTEM
- K885294 — BORRELIA BURGDORFERI IGM ANTIBODY TEST SYSTEM
- K883083 — MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM
- K873114 — CYTOMEGALOVIRUS CONTROL SLIDES
- K872082 — RESPIRATORY SYNCYTIAL VIRUS CONTROL SLIDE
- K864006 — LEGIONELLA PNEUMOPHILA SER. 1 ANTIGEN LATEX TEST
- K862630 — MYCOPLASMA PNEUMONIAE ANTIBODY LATEX TEST SYSTEM
- K854108 — POLYVALENT FLUORESCENT ANTIBODY REAGENTS FOR LEGIO
Data sourced from openFDA. This site is unofficial and independent of the FDA.