FDA 510(k) Application Details - K161574

Device Classification Name System, Tomography, Computed, Emission

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510(K) Number K161574
Device Name System, Tomography, Computed, Emission
Applicant GE Medical Systems, L.L.C.
3000 N Grandview Blvd
Waukesha, WI 53188 US
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Contact Helen Peng
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Regulation Number 892.1200

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Classification Product Code KPS
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Date Received 06/07/2016
Decision Date 08/11/2016
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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