FDA 510(k) Applications Submitted by COMPUMEDICS USA, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K081151 04/23/2008 COMPUMEDICS NEUVO COMPUMEDICS USA, LTD.
K040194 01/28/2004 COMPUMEDICS SUMMIT IP COMPUMEDICS USA, LTD.
K033052 09/29/2003 CONDUCTIVE EEG ELECTROLYTE COMPUMEDICS USA, LTD.


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