Diagnostic Products Corporation is one of 23883 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diagnostic Products Corporation - FDA 510(k) Cleared Devices
Recent clearances: IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP, IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6, IMMULITE/IMMULITE 1000 TURBO INTACT PTH
3
Total
3
Cleared
0
Denied
Diagnostic Products Corporation has 3 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 3 cleared submissions from 2006 to 2006. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Diagnostic Products Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diagnostic Products Corporation
3 devices