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FDA 510(k) Application Details - K151598
Device Classification Name
More FDA Info for this Device
510(K) Number
K151598
Device Name
VesselNavigator Rel. 1.0
Applicant
PHILIPS MEDICAL SYSTEMS NEDERLAND BV
VEENPLUIS 4-6
BEST 5684PC NL
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Contact
LISELOTTE KORNMANN
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Regulation Number
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Classification Product Code
OWB
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Date Received
06/12/2015
Decision Date
08/17/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
N
Expedited Review
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