LiteWalk— 510(k) K192607

Substantially Equivalent

Viasonix , Ltd.

FDA 510(k) clearance K192607 for LiteWalk, Substantially Equivalent on 2019-12-19. Applicant: Viasonix , Ltd..

Clearance details

Applicant: Viasonix , Ltd.
Product code: Code IRP
Advisory panel: Physical Medicine
Date received: 2019-09-20
Decision date: 2019-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ra'Anana, IL

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