UV Active Implant System
K-Number: K182194 · 2018-12-14
ApplicantDio Corporation
Decision Date2018-12-14
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
UV Active Implant System is a medical device manufactured by Dio Corporation. It received FDA 510(k) clearance on 2018-12-14 under approval number K182194. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the UV Active Implant System?
UV Active Implant System is a medical device that received FDA 510(k) clearance on 2018-12-14. It is manufactured by Dio Corporation. The 510(k) number is K182194.
When was UV Active Implant System approved by the FDA?
UV Active Implant System received FDA 510(k) clearance on 2018-12-14, under approval number K182194.
What company makes UV Active Implant System?
UV Active Implant System is manufactured by Dio Corporation.
What is the FDA product code for UV Active Implant System?
The FDA product code for UV Active Implant System is DZE.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.