Neuro Assessment System NAS-1000— 510(k) K172892

Name: FDA 510(k) clearance K172892
Creator: U.S. Food and Drug Administration
Published: 2018-03-08

Substantially Equivalent

Headsense Medical, Inc.

FDA 510(k) clearance K172892 for Neuro Assessment System NAS-1000, Substantially Equivalent on 2018-03-08. Applicant: Headsense Medical, Inc.. Device class: 2.

Clearance details

Applicant: Headsense Medical, Inc.
Product code: Code QBE
Device class: Class 2
Regulation: 21 CFR 870.1875
Advisory panel: Cardiovascular
Date received: 2017-09-22
Decision date: 2018-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Akron, OH, US

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