FDA 510(k), K132108, MAXIO
FDA 510(k), K132108, MAXIO
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510(K) Number: K132108
Device Name: MAXIO
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 07/08/2013
Decision Date: 05/19/2014
Regulation Medical Specialty: Radiology
Device Name: MAXIO
Manufacturer:
Device Classification Name: System, X-Ray, Tomography, Computed
Regulation Number: 892.1750
Classification Product Code: JAK
Date Received: 07/08/2013
Decision Date: 05/19/2014
Regulation Medical Specialty: Radiology