Persyst Mobile App— 510(k) K171184

Name: FDA 510(k) clearance K171184
Creator: U.S. Food and Drug Administration
Published: 2017-09-21

Substantially Equivalent

Persyst Development Corporation

FDA 510(k) clearance K171184 for Persyst Mobile App, Substantially Equivalent on 2017-09-21. Applicant: Persyst Development Corporation. Device class: 2.

Clearance details

Applicant: Persyst Development Corporation
Product code: Code OMB
Device class: Class 2
Regulation: 21 CFR 882.1400
Advisory panel: Neurology
Date received: 2017-04-24
Decision date: 2017-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Solana Beach, CA, US

Download summary PDF View on FDA.gov ↗

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