NICO BrainPath— 510(k) K172433

Substantially Equivalent

Nico Corporation

FDA 510(k) clearance K172433 for NICO BrainPath, Substantially Equivalent on 2017-09-07. Applicant: Nico Corporation. Device class: 2.

Clearance details

Applicant
Nico Corporation
Product code
Code GZT
Device class
Class 2
Regulation
21 CFR 882.4800
Advisory panel
Neurology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Indianapolis, IN, US
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