510(k) K250239

Device
NeuroMatch
Applicant
LVIS Corporation
510(k) number
K250239
Product code
OLX
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-23
Date received
2025-01-27
Regulation
882.1400
Classification name
Source Localization Software For Electroencephalograph Or Magnetoencephalograph
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Sweta Srivastava
Address
2600 E Bayshore Rd. Palo Alto CA US 94303 94303

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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