Automatic Registration
K-Number: K234047 · 2024-03-20
ApplicantBrainlab AG
Decision Date2024-03-20
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Automatic Registration is a medical device manufactured by Brainlab AG. It received FDA 510(k) clearance on 2024-03-20 under approval number K234047. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Automatic Registration?
Automatic Registration is a medical device that received FDA 510(k) clearance on 2024-03-20. It is manufactured by Brainlab AG. The 510(k) number is K234047.
When was Automatic Registration approved by the FDA?
Automatic Registration received FDA 510(k) clearance on 2024-03-20, under approval number K234047.
What company makes Automatic Registration?
Automatic Registration is manufactured by Brainlab AG.
What is the FDA product code for Automatic Registration?
The FDA product code for Automatic Registration is OLO.
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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.