FDA 510(k) Applications Submitted by QUANTECH LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K990258 | 01/27/1999 | QUANTECH TOTAL B-HCG ASSAY | QUANTECH LTD. |
| K012943 | 08/31/2001 | THE QUANTECH FASTRAQ AUTOMATED ANALYZER, AND THE QUANTECH PREPAQ TOTAL HCG TEST CARTRIDGE | QUANTECH LTD. |
| K984433 | 12/14/1998 | QUANTECH CK-MB ASSAY | QUANTECH LTD. |
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