Diagnostic Products Corporation
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K063057 | IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP | NQD | 2006-12-22 | View |
| 510(k) | K060929 | IMMULITE 2500 VITAMIN B12 MODEL L5KVB2-200 TEST,L5KVB6-600 TEST, IMMULITE 2500 FOLIC ACID MODEL L5KFO2-200 TEST,L5KFO6-6 | CDD | 2006-04-28 | View |
| 510(k) | K053533 | IMMULITE/IMMULITE 1000 TURBO INTACT PTH | CEW | 2006-02-03 | View |
No matching devices.
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