July 6, 2010 (Rockville, MD) — The US Food and Drug Administration (FDA) has issued a class 1 recall of the LIFEPAK 20 and LIFEPAK 20e external defibrillator/monitors (Physio-Control, Redmond, WA) [1] ...
CodeManagement Module for LIFEPAK 20/20e, LIFENET System and CODE-STAT work together to help improve in-hospital cardiac arrest outcomes REDMOND, Wash.--(BUSINESS WIRE)--Physio-Control, the leading ...
CodeManagement Module for LIFEPAK 20/20e, LIFENET System and CODE-STAT work together to help improve in-hospital cardiac arrest outcomes Physio-Control, Inc.Jennifer Roth, 425-867-4393orErik Denny, ...
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