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FDA 510(k) Applications Submitted by MARK PERKINS
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072527
09/07/2007
AUTOPULSE RESUSCITATION SYSTEM, MODEL 100
ZOLL CIRCULATION
K063602
12/04/2006
AUTOPULSE RESUSCITATION SYSTEM MODEL100
ZOLL CIRCULATION
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