Elite Diagnostic , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Elite Diagnostic , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Elite Diagnostic , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 5 cleared submissions from 1989 to 1989. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Elite Diagnostic , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Elite Diagnostic , Ltd.
5 devices
Cleared
Apr 21, 1989
EDL GLOBAL ACTIVATED PARTIAL THROMBOPLASTIN TIME
Hematology
59d
Cleared
Apr 21, 1989
EDL ONE-STAGE PROTHROMBIN TIME REAGENT
Hematology
43d
Cleared
Apr 10, 1989
EDL ABNORMAL COAGULATION CONTROL
Hematology
35d
Cleared
Apr 10, 1989
EDL NORMAL COAGULATION CONTROL
Hematology
35d
Cleared
Mar 15, 1989
EDL ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT
Hematology
36d