FDA 510(k), K111346, RESOLUTIONMD MOBILE MODEL RMB-MOB-2X

FDA 510(k), K111346, RESOLUTIONMD MOBILE MODEL RMB-MOB-2X

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510(K) Number: K111346
Device Name: RESOLUTIONMD MOBILE MODEL RMB-MOB-2X
Manufacturer: KYLE PETERSON
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 05/13/2011
Date Received: 09/09/2011
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
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