FDA 510(k) Application Details - K974707

Device Classification Name System, Digital Image Communications, Radiological

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510(K) Number K974707
Device Name System, Digital Image Communications, Radiological
Applicant VISUAL MED, INC.
3695 CENTRE CIRCLE DR.
FT. MILL, SC 29715 US
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Regulation Number 892.2020

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Classification Product Code LMD
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Date Received 12/16/1997
Decision Date 07/31/1998
Decision SESE - SUBST EQUIV
Classification Advisory Committee RA - Radiology
Review Advisory Committee RA - Radiology
Statement / Summary / Purged Status Statement
Type Traditional
Reviewed By Third Party N
Expedited Review



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