Medical Diagnostic Technologies, Inc. - FDA 510(k) Cleared Devices
57
Total
57
Cleared
0
Denied
Medical Diagnostic Technologies, Inc. has 57 FDA 510(k) cleared medical devices. Based in Augusta, US.
Historical record: 57 cleared submissions from 1985 to 2006. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Medical Diagnostic Technologies, Inc. Filter by specialty or product code using the sidebar.
57 devices
Cleared
Sep 11, 2006
CTC WORKSTATION, MODEL 2200
Radiology
40d
Cleared
Aug 12, 1997
SPECTROLYSE HEPARIN (ANTI-IIA)
Hematology
62d
Cleared
Nov 18, 1996
CHROMOLIZE PAI-1 KIT
Hematology
98d
Cleared
Aug 14, 1996
SPECTROLYSE ANTITHROMBIN III (ANTI-XA)
Hematology
163d
Cleared
Jul 31, 1996
CHROMOLIZE TPA ASSAY KIT
Hematology
35d
Cleared
Jun 05, 1996
TINTELIZE PAI-1 KIT
Hematology
126d
Cleared
Jun 03, 1996
U-DOA CONTROLS
Toxicology
31d
Cleared
May 24, 1996
LA POSITIVE CONTROL PLASMA
Hematology
45d
Cleared
Apr 03, 1996
VENOM TIEM REAGENT
Hematology
146d
Cleared
Feb 29, 1996
BIOCLOT PROTEIN S
Hematology
76d
Cleared
Nov 27, 1995
ALKALINE PHOSPHATASE REAGENT SYSTEM
Chemistry
164d
Cleared
Sep 29, 1995
ASPARTATE AMINOTRANSFERASE REAGENT SYSTEM
Chemistry
105d
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