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FDA 510(k) Application Details - K020715
Device Classification Name
Automated External Defibrillators (Non-Wearable)
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510(K) Number
K020715
Device Name
Automated External Defibrillators (Non-Wearable)
Applicant
PHILIPS MEDICAL SYSTEMS
2301 FIFTH AVE., SUITE 200
SEATTLE, WA 98121 US
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Contact
TAMARA YOUNT
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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
03/05/2002
Decision Date
11/08/2002
Decision
ST - Substantially Equivalent - Subject to Tracking Reg.
Classification Advisory Committee
CV - Cardiovascular
Review Advisory Committee
CV - Cardiovascular
Statement / Summary / Purged Status
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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