Erchonia CLX (Model # CFL)
K-Number: K252574 · 2025-12-15
ApplicantErchonia Corporation
Decision Date2025-12-15
Product CodeOLI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Erchonia CLX (Model # CFL) is a medical device manufactured by Erchonia Corporation. It received FDA 510(k) clearance on 2025-12-15 under approval number K252574. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Erchonia CLX (Model # CFL)?
Erchonia CLX (Model # CFL) is a medical device that received FDA 510(k) clearance on 2025-12-15. It is manufactured by Erchonia Corporation. The 510(k) number is K252574.
When was Erchonia CLX (Model # CFL) approved by the FDA?
Erchonia CLX (Model # CFL) received FDA 510(k) clearance on 2025-12-15, under approval number K252574.
What company makes Erchonia CLX (Model # CFL)?
Erchonia CLX (Model # CFL) is manufactured by Erchonia Corporation.
What is the FDA product code for Erchonia CLX (Model # CFL)?
The FDA product code for Erchonia CLX (Model # CFL) is OLI.
Related Clinical Trials
Other Devices by Erchonia Corporation
Related Devices (Code: OLI)
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.