ClearanceBrief
510(k) K063602 ยท DRM Compressor, Cardiac, External

AUTOPULSE RESUSCITATION SYSTEM MODEL100

ApplicantZoll Circulation, Sunnyvale CA, US
DecisionSubstantially Equivalent, Dec 21, 2006
ReceivedDec 4, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K063602

DateFirm and productCodeLinked 510(k)
Jan 9, 2013Zoll Circulation, Inc.
AutoPulse Resuscitation System Model 100, Mfg by:Zoll Circulation Sunnyvale, CA. The AutoPulse Model 100 Automatic Mechanical Chest compressor is intended to be used as an adjunct to manual CPR, on
Terminated
DRMNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.