FDA 510(k)

Sourcerer

K-Number: K241513 · 2024-09-27

ApplicantBrain Electrophysiology Laboratory Company, LLC

Decision Date2024-09-27

Product CodeOLX

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Sourcerer is the device name listed in this FDA 510(k) record. The listed applicant is Brain Electrophysiology Laboratory Company, LLC. It received FDA 510(k) clearance on 2024-09-27 under 510(k) 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. The listed applicant is Brain Electrophysiology Laboratory Company, LLC. The 510(k) number is K241513.

When did Sourcerer receive FDA 510(k) clearance?

Sourcerer received FDA 510(k) clearance on 2024-09-27, under 510(k) number K241513.

Who is the listed applicant for Sourcerer?

The FDA 510(k) record lists Brain Electrophysiology Laboratory Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sourcerer?

The FDA product code for Sourcerer is OLX.

Other records listing Brain Electrophysiology Laboratory Company, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250058NEAT 001

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.