FDA 510(k) Applications for Medical Device Product Code "NAL"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K990258 | QUANTECH LTD. | QUANTECH TOTAL B-HCG ASSAY | 12/21/1999 |
K012943 | QUANTECH LTD. | THE QUANTECH FASTRAQ AUTOMATED ANALYZER, AND THE QUANTECH PREPAQ TOTAL HCG TEST CARTRIDGE | 01/18/2002 |