ClearanceBrief
510(k) K072527 ยท DRM Compressor, Cardiac, External

AUTOPULSE RESUSCITATION SYSTEM, MODEL 100

ApplicantZoll Circulation, Sunnyvale CA, US
DecisionSubstantially Equivalent, Mar 19, 2008
ReceivedSep 7, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072527

DateFirm and productCodeLinked 510(k)
Apr 7, 2011Zoll Circulation, Inc.
Zoll Auto Pulse Resuscitation System; Zoll Circulation Inc., Sunnyvale, CA 94085 Cardiac Compressor used as an adjunct to manual CPR. Use of AutoPulse is intended to reduce the impact of rescuer fati
Terminated
DRMNone listed

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