Medical Diagnostic Technologies, Inc.
Medical Diagnostic Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1985, most recent 2006.
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.