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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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