VERABAND
K-Number: K233987 · 2024-06-17
ApplicantArbor Medical Innovations, LLC
Decision Date2024-06-17
Product CodeLEL
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
VERABAND is a medical device manufactured by Arbor Medical Innovations, LLC. It received FDA 510(k) clearance on 2024-06-17 under approval number K233987. The device is classified under product code LEL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VERABAND?
VERABAND is a medical device that received FDA 510(k) clearance on 2024-06-17. It is manufactured by Arbor Medical Innovations, LLC. The 510(k) number is K233987.
When was VERABAND approved by the FDA?
VERABAND received FDA 510(k) clearance on 2024-06-17, under approval number K233987.
What company makes VERABAND?
VERABAND is manufactured by Arbor Medical Innovations, LLC.
What is the FDA product code for VERABAND?
The FDA product code for VERABAND is LEL.
Related Devices (Code: LEL)
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.