LVIS NeuroMatch— 510(k) K222450

Substantially Equivalent

LVIS Corporation

FDA 510(k) clearance K222450 for LVIS NeuroMatch, Substantially Equivalent on 2023-06-09. Applicant: LVIS Corporation.

Clearance details

Applicant
LVIS Corporation
Product code
Code OMB
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Palo Alto, CA, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.