FDA 510(k) Application Details - K062451

Device Classification Name System, X-Ray, Tomography, Computed

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510(K) Number K062451
Device Name System, X-Ray, Tomography, Computed
Applicant NEUSOFT MEDICAL SYSTEMS CO., LTD.
NO.3-11, WENHUA ROAD
HEPING DISTRICT
SHENYANG, LIAONING 110004 CN
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Contact TIAN YANFANG
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Regulation Number 892.1750

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Classification Product Code JAK
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Date Received 08/22/2006
Decision Date 09/28/2006
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

FDA Source Information for K062451


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