FDA 510(k) Applications Submitted by Physio-Control, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K182503 09/12/2018 Sterilizable Internal Defibrillation Paddles for use with LIFEPAK defibrillators/monitors Physio-Control, Inc.
K130454 02/22/2013 LIFEPAK 20 DEFIBRILLATOR/MONITOR, LIFEPAK 20E DEFIBRILLATOR/MONITOR PHYSIO-CONTROL, INC.
K122600 08/27/2012 LIFEPAK 1000 DEFIBRILLATOR PHYSIO-CONTROL, INC.
K102972 10/06/2010 LIFEPAK 12 PHYSIO-CONTROL, INC.
K073089 11/01/2007 LIFEPAK 20E PHYSIO-CONTROL, INC.
K103567 12/06/2010 LIFEPAK 15 MONITOR/DEFIBRILLATOR PHYSIO-CONTROL, INC.
K142430 08/29/2014 LIFEPAK 15 monitor/defibrillator PHYSIO-CONTROL, INC.
K102757 09/23/2010 LIFENET SYSTEM PHYSIO-CONTROL, INC.
K082937 10/01/2008 LIFEPAK 15 MONITOR/DEFIBRILLATOR PHYSIO-CONTROL, INC.
K123597 11/21/2012 TRUECPR COACHING DEVICE PHYSIO-CONTROL, INC.
K093925 12/22/2009 LIFENET SYSTEM PHYSIO-CONTROL, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact