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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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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