FDA 510(k) Applications Submitted by MEGA ELECTRONICS LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K131699 06/11/2013 EMOTION ECG MOBILE MEGA ELECTRONICS LTD.
K993411 10/12/1999 FEMISCAN CLINIC SYSTEM, MODEL FS-ICTRA AND FEMISCAN PERSONAL SYSTEM, MODEL FS-HMTR MEGA ELECTRONICS LTD.
K963202 08/15/1996 MEGA ME 3000 PROFESSIONAL MUSCLE TESTER MEGA ELECTRONICS LTD.
K143032 10/22/2014 eMotion Faros ECG Mobile MEGA ELECTRONICS LTD.


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