FDA 510(k) Applications Submitted by NICK MENDISE

FDA 510(k) Number Submission Date Device Name Applicant
K103159 10/26/2010 CARDIO MED MODEL A102, H104, O101, P103, AND Z100 CARDIO MEDICAL PRODUCTS, INC.
K103334 11/15/2010 CARDIO MED CARDIO MEDICAL PRODUCTS, INC.
K103651 12/14/2010 CARDIOMED CARDIO MEDICAL PRODUCTS, INC.


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