FDA 510(k) Applications for Medical Device Product Code "DRK"
(Dc-Defibrillator, High Energy, (Including Paddles))

FDA 510(k) Number Applicant Device Name Decision Date
K934067 NATIONAL CUSTOM ENT., INC. POWRPAK REPLACEMENT BATTERIES FOR PHISIO-CONTROL LIFEPAK 5/10 10/07/1993


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