Biorent Diagnostic, Inc.
FDA 510(k) & PMA Approved Devices — 11 products
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Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K832747 | ALBUMIN REAGENT SET | CIX | 1983-10-14 | View |
| 510(k) | K823211 | CK-UV REAGENT | JHS | 1982-11-22 | View |
| 510(k) | K823060 | HEMOGLOBIN REAGENT | KHG | 1982-11-22 | View |
| 510(k) | K822494 | OPTIMIZED UV-GPT REAGENT SET | CKA | 1982-09-21 | View |
| 510(k) | K822493 | OPTIMIZED UV-GOT REAGENT SET | CIT | 1982-09-21 | View |
| 510(k) | K822492 | OPTIMIZED UV-LDH REAGENT SET | CFJ | 1982-09-17 | View |
| 510(k) | K820768 | COLORIMETRIC LDH REAGENT SET | CFH | 1982-04-14 | View |
| 510(k) | K820632 | COLORIMETRIC URIC ACID REAGENT SET | KNK | 1982-03-25 | View |
| 510(k) | K813555 | GLUCOSE ENZYME-COLOR REAGENT SET | CGA | 1982-01-18 | View |
| 510(k) | K813244 | UV URIC ACID DETERMINATION | CDO | 1981-12-08 | View |
| 510(k) | K811760 | CHOLESTEROL DETERMINATION | CHH | 1981-07-10 | View |
No matching devices.
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