Sonic DL
K-Number: K223523 · 2023-05-30
Decision Date2023-05-30
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Sonic DL is a medical device manufactured by Ge Medical Systems,Llc (Ge Healthcare). It received FDA 510(k) clearance on 2023-05-30 under approval number K223523. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Sonic DL?
Sonic DL is a medical device that received FDA 510(k) clearance on 2023-05-30. It is manufactured by Ge Medical Systems,Llc (Ge Healthcare). The 510(k) number is K223523.
When was Sonic DL approved by the FDA?
Sonic DL received FDA 510(k) clearance on 2023-05-30, under approval number K223523.
What company makes Sonic DL?
Sonic DL is manufactured by Ge Medical Systems,Llc (Ge Healthcare).
What is the FDA product code for Sonic DL?
The FDA product code for Sonic DL is LNH.
Other Devices by Ge Medical Systems,Llc (Ge Healthcare)
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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.