nordicDSC
K-Number: K212720 · 2022-03-03
ApplicantNordicneurolab AS
Decision Date2022-03-03
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
nordicDSC is a medical device manufactured by Nordicneurolab AS. It received FDA 510(k) clearance on 2022-03-03 under approval number K212720. 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 nordicDSC?
nordicDSC is a medical device that received FDA 510(k) clearance on 2022-03-03. It is manufactured by Nordicneurolab AS. The 510(k) number is K212720.
When was nordicDSC approved by the FDA?
nordicDSC received FDA 510(k) clearance on 2022-03-03, under approval number K212720.
What company makes nordicDSC?
nordicDSC is manufactured by Nordicneurolab AS.
What is the FDA product code for nordicDSC?
The FDA product code for nordicDSC 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.