FDA 510(k), K083691, BONEVUE
FDA 510(k), K083691, BONEVUE
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$149.00 USD
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510(K) Number: K083691
Device Name: BONEVUE
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/12/2008
Decision Date: 02/25/2009
Regulation Medical Specialty: Radiology
Device Name: BONEVUE
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 12/12/2008
Decision Date: 02/25/2009
Regulation Medical Specialty: Radiology