FDA 510(k) Applications Submitted by COMDEK INDUSTRIAL CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K083351 11/13/2008 PROABLE PULSE OXIMETER, MODEL MD-600P, TRAVELER OXIMETER, MODEL MD-650P AND PALM PULSE OXIMETER, MODEL MD-680P COMDEK INDUSTRIAL CORP.


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