FDA 510(k), K151988, Visible Patient Suite
FDA 510(k), K151988, Visible Patient Suite
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$149.00 USD
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510(K) Number: K151988
Device Name: Visible Patient Suite
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 07/17/2015
Decision Date: 10/15/2015
Regulation Medical Specialty: Radiology
Device Name: Visible Patient Suite
Manufacturer:
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 07/17/2015
Decision Date: 10/15/2015
Regulation Medical Specialty: Radiology