FDA 510(k), K120187, MULTI-MODALITY IMAGE FUSION

FDA 510(k), K120187, MULTI-MODALITY IMAGE FUSION

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510(K) Number: K120187
Device Name: MULTI-MODALITY IMAGE FUSION
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 01/23/2012
Decision Date: 04/06/2012
Regulation Medical Specialty: Radiology
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