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FDA 510(k) Applications for Medical Device Product Code "LNW"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K960648 | FEMTEK, INC. | PHEM-CHEK | 05/13/1996 |
K012230 | FEMTEK,LLC. | PHEM-ALERT | 10/09/2001 |
K032161 | FEMTEK,LLC. | PHEM-ALERT | 09/30/2003 |