EON
K-Number: K222226 · 2023-02-17
Decision Date2023-02-17
Product CodePKT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
EON is a medical device manufactured by Dominion Aesthetic Technologies, Inc.. It received FDA 510(k) clearance on 2023-02-17 under approval number K222226. The device is classified under product code PKT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the EON?
EON is a medical device that received FDA 510(k) clearance on 2023-02-17. It is manufactured by Dominion Aesthetic Technologies, Inc.. The 510(k) number is K222226.
When was EON approved by the FDA?
EON received FDA 510(k) clearance on 2023-02-17, under approval number K222226.
What company makes EON?
EON is manufactured by Dominion Aesthetic Technologies, Inc..
What is the FDA product code for EON?
The FDA product code for EON is PKT.
Other Devices by Dominion Aesthetic Technologies, Inc.
Related Devices (Code: PKT)
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.