FDA 510(k) Application Details - K040141

Device Classification Name System, Tomography, Computed, Emission

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510(K) Number K040141
Device Name System, Tomography, Computed, Emission
Applicant SYNTERMED, INC.
3340 PEACHTREE RD NE
SUITE 1800
ATLANTA, GA 30326 US
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Contact KENNETH F VAN TRAIN
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Regulation Number 892.1200

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Classification Product Code KPS
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Date Received 01/22/2004
Decision Date 01/30/2004
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 Y
Expedited Review



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