Erchonia EVRL
K-Number: K251843 · 2025-09-12
ApplicantErchonia Corporation
Decision Date2025-09-12
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Erchonia EVRL is a medical device manufactured by Erchonia Corporation. It received FDA 510(k) clearance on 2025-09-12 under approval number K251843. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Erchonia EVRL?
Erchonia EVRL is a medical device that received FDA 510(k) clearance on 2025-09-12. It is manufactured by Erchonia Corporation. The 510(k) number is K251843.
When was Erchonia EVRL approved by the FDA?
Erchonia EVRL received FDA 510(k) clearance on 2025-09-12, under approval number K251843.
What company makes Erchonia EVRL?
Erchonia EVRL is manufactured by Erchonia Corporation.
What is the FDA product code for Erchonia EVRL?
The FDA product code for Erchonia EVRL is OLP.
Related Clinical Trials
Other Devices by Erchonia Corporation
Related Devices (Code: OLP)
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.