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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name automated external defibrillators (non-wearable)
510(k) Number K122600
Device Name LIFEPAK 1000 DEFIBRILLATOR
Applicant
PHYSIO-CONTROL, INC.
11811 WILLOWS RD., N.E.
PO BOX 97006
REDMOND,  WA  98073 -9706
Applicant Contact MICHELLE ACKERMANN
Correspondent
PHYSIO-CONTROL, INC.
11811 WILLOWS RD., N.E.
PO BOX 97006
REDMOND,  WA  98073 -9706
Correspondent Contact MICHELLE ACKERMANN
Regulation Number870.5310
Classification Product Code
MKJ  
Date Received08/27/2012
Decision Date 10/11/2012
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Cardiovascular
510k Review Panel Cardiovascular
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
Recalls CDRH Recalls
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