Neurolutions Upper Extremity Rehabilitation System— 510(k) DEN200046

Name: FDA 510(k) clearance DEN200046
Creator: U.S. Food and Drug Administration
Published: 2021-04-23

Unknown

Neurolutions, Inc.

FDA 510(k) clearance DEN200046 for Neurolutions Upper Extremity Rehabilitation System, Unknown on 2021-04-23. Applicant: Neurolutions, Inc.. Device class: 2.

Clearance details

Applicant: Neurolutions, Inc.
Product code: Code QOL
Device class: Class 2
Regulation: 21 CFR 890.5420
Advisory panel: Neurology
Date received: 2020-07-23
Decision date: 2021-04-23
Decision: Unknown
Clearance type: Direct
Location: Santa Cruz, CA, US

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