nordicMEDiVA
K-Number: K241608 · 2024-06-28
ApplicantNordicneurolab AS
Decision Date2024-06-28
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
nordicMEDiVA is a medical device manufactured by Nordicneurolab AS. It received FDA 510(k) clearance on 2024-06-28 under approval number K241608. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the nordicMEDiVA?
nordicMEDiVA is a medical device that received FDA 510(k) clearance on 2024-06-28. It is manufactured by Nordicneurolab AS. The 510(k) number is K241608.
When was nordicMEDiVA approved by the FDA?
nordicMEDiVA received FDA 510(k) clearance on 2024-06-28, under approval number K241608.
What company makes nordicMEDiVA?
nordicMEDiVA is manufactured by Nordicneurolab AS.
What is the FDA product code for nordicMEDiVA?
The FDA product code for nordicMEDiVA is LLZ.
Other Devices by Nordicneurolab AS
Related Devices (Code: LLZ)
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.