FDA 510(k) Applications Submitted by FEMTEK,LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K032161 07/15/2003 PHEM-ALERT FEMTEK,LLC.
K012230 07/16/2001 PHEM-ALERT FEMTEK,LLC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact