Quantech , Ltd.
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) | K012943 | THE QUANTECH FASTRAQ AUTOMATED ANALYZER, AND THE QUANTECH PREPAQ TOTAL HCG TEST CARTRIDGE | NAL | 2002-01-18 | View |
| 510(k) | K990258 | QUANTECH TOTAL B-HCG ASSAY | NAL | 1999-12-21 | View |
| 510(k) | K984433 | QUANTECH CK-MB ASSAY | MYT | 1999-11-01 | View |
No matching devices.
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