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FDA 510(k), K182194, UV Active Implant System
FDA 510(k), K182194, UV Active Implant System
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$89.00 USD
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510(K) Number: K182194
Device Name: UV Active Implant System
Manufacturer: DIO Corporation
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 08/14/2018
Decision Date: 12/14/2018
Regulation Medical Specialty: Dental
Device Name: UV Active Implant System
Manufacturer: DIO Corporation
Device Classification Name: implant, endosseous, root-form
Regulation Number: 872.3640
Classification Product Code: DZE
Date Received: 08/14/2018
Decision Date: 12/14/2018
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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