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FDA 510(k) Application Details - K161674
Device Classification Name
System, Tomography, Computed, Emission
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510(K) Number
K161674
Device Name
System, Tomography, Computed, Emission
Applicant
DDD-DIAGNOSTIC A/S
DR. NEERGAARDS VEJ 5E
HORSHOLM 2970 DK
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Contact
Niels Sorensen
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Regulation Number
892.1200
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Classification Product Code
KPS
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More FDA Info for this Product Code
Date Received
06/16/2016
Decision Date
10/20/2016
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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