FDA 510(k) Application Details - K173547

Device Classification Name System, Tomography, Computed, Emission

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510(K) Number K173547
Device Name System, Tomography, Computed, Emission
Applicant Cardiovascular Imaging Technologies
4320 Wornall Road, Suite 114
Kansas City, UT 64111 US
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Contact James A. Case
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Regulation Number 892.1200

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Classification Product Code KPS
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Date Received 11/16/2017
Decision Date 01/12/2018
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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