FDA 510(k) Application Details - K243605

Device Classification Name System, Tomography, Computed, Emission

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510(K) Number K243605
Device Name System, Tomography, Computed, Emission
Applicant GE Medical Systems Israel, Functional Imaging
(GE Healthcare)
4 Hayozma Street
Tirat HaCarmel 30200 IL
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Contact Hanne Jubran
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Regulation Number 892.1200

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Classification Product Code KPS
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Date Received 11/21/2024
Decision Date 01/17/2025
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

FDA Source Information for K243605


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