Sourcerer
K-Number: K241513 · 2024-09-27
Decision Date2024-09-27
Product CodeOLX
Advisory CommitteeNE
DecisionSubstantially Equivalent
Device Summary
Sourcerer is a medical device manufactured by Brain Electrophysiology Laboratory Company, LLC. It received FDA 510(k) clearance on 2024-09-27 under approval number K241513. The device is classified under product code OLX. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Sourcerer?
Sourcerer is a medical device that received FDA 510(k) clearance on 2024-09-27. It is manufactured by Brain Electrophysiology Laboratory Company, LLC. The 510(k) number is K241513.
When was Sourcerer approved by the FDA?
Sourcerer received FDA 510(k) clearance on 2024-09-27, under approval number K241513.
What company makes Sourcerer?
Sourcerer is manufactured by Brain Electrophysiology Laboratory Company, LLC.
What is the FDA product code for Sourcerer?
The FDA product code for Sourcerer is OLX.
Other Devices by Brain Electrophysiology Laboratory Company, LLC
Related Devices (Code: OLX)
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.