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FDA 510(k), K150912, Houva-NET Control System
FDA 510(k), K150912, Houva-NET Control System
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510(K) Number: K150912
Device Name: Houva-NET Control System
Manufacturer: National Biological Corporation
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 04/03/2015
Decision Date: 07/10/2015
Regulation Medical Specialty: General & Plastic Surgery
Device Name: Houva-NET Control System
Manufacturer: National Biological Corporation
Device Classification Name: light, ultraviolet, dermatological
Regulation Number: 878.4630
Classification Product Code: FTC
Date Received: 04/03/2015
Decision Date: 07/10/2015
Regulation Medical Specialty: General & Plastic Surgery
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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