FDA 510(k) Application Details - K031248

Device Classification Name System, Image Processing, Radiological

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510(K) Number K031248
Device Name System, Image Processing, Radiological
Applicant MIRAMEDICA, INC
15466 LOS GATOS BLVD.
SUITE 109, PMB #171
LOS GATOS, CA 95032 US
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Contact WIDO MENHARDT
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Regulation Number 892.2050

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Classification Product Code LLZ
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Date Received 04/18/2003
Decision Date 06/20/2003
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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