Elite Diagnostic , Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K890859 | EDL GLOBAL ACTIVATED PARTIAL THROMBOPLASTIN TIME | GFO | 1989-04-21 | View |
| 510(k) | K891370 | EDL ONE-STAGE PROTHROMBIN TIME REAGENT | GJS | 1989-04-21 | View |
| 510(k) | K891175 | EDL ABNORMAL COAGULATION CONTROL | GGL | 1989-04-10 | View |
| 510(k) | K891179 | EDL NORMAL COAGULATION CONTROL | GIZ | 1989-04-10 | View |
| 510(k) | K890619 | EDL ACTIVATED PARTIAL THROMBOPLASTIN TIME REAGENT | GFO | 1989-03-15 | View |
No matching devices.
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