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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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