DYNAMIC NEUROSCREENING DEVICE— 510(k) K141208

Substantially Equivalent

Prosenex

FDA 510(k) clearance K141208 for DYNAMIC NEUROSCREENING DEVICE, Substantially Equivalent on 2014-07-23. Applicant: Prosenex.

Clearance details

Applicant: Prosenex
Product code: Code LQW
Advisory panel: Neurology
Date received: 2014-05-09
Decision date: 2014-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Leola, PA, US

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