FDA 510(k) Application Details - K001276

Device Classification Name System, Tomography, Computed, Emission

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510(K) Number K001276
Device Name System, Tomography, Computed, Emission
Applicant SYNTERMED, INC.
210 INTERSTATE NORTH PKWY.
SUITE 700
ATLANTA, GA 30339 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 04/21/2000
Decision Date 07/17/2000
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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