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FDA 510(k) Application Details - K042404
Device Classification Name
Automated External Defibrillators (Non-Wearable)
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510(K) Number
K042404
Device Name
Automated External Defibrillators (Non-Wearable)
Applicant
MEDTRONIC EMERGENCY RESPONSE SYSTEMS, INC.
11811 WILLOWS RD., N.E.
PO BOX 97006
REDMOND, WA 98073 US
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Contact
SHERRI POCOCK
Other 510(k) Applications for this Contact
Regulation Number
870.5310
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Classification Product Code
MKJ
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More FDA Info for this Product Code
Date Received
09/03/2004
Decision Date
12/22/2005
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Summary
Type
Traditional
Reviewed By Third Party
N
Expedited Review
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