Medical Diagnostic Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Medical Diagnostic Technologies, Inc.
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
Looking for a specific device from Medical Diagnostic...? Search by device name or K-number.
Search all Medical Diagnostic... devices