FDA 510(k) Applications for Medical Device Product Code "LNW"
(Paper, Obstetric Ph)

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


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