FDA 510(k), K160147, CT TrueView
FDA 510(k), K160147, CT TrueView
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$149.00 USD
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510(K) Number: K160147
Device Name: CT TrueView
Manufacturer:
Device Classification Name: Interventional Fluoroscopic X-Ray System
Regulation Number: 892.1650
Classification Product Code: OWB
Date Received: 01/21/2016
Decision Date: 08/10/2016
Regulation Medical Specialty: Radiology
Device Name: CT TrueView
Manufacturer:
Device Classification Name: Interventional Fluoroscopic X-Ray System
Regulation Number: 892.1650
Classification Product Code: OWB
Date Received: 01/21/2016
Decision Date: 08/10/2016
Regulation Medical Specialty: Radiology