FDA 510(k) Applications Submitted by Viasonix Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K170859 03/22/2017 Dolphin/IQ and Dolphin/4D Viasonix Ltd.
K202742 09/18/2020 Dolphin/IQ, Dolphin/4D and Dolphin/MAX with Dolphin/XF robot accessory Viasonix Ltd.
K191023 04/17/2019 Dolphin/IQ, Dolphin/4D and Dolphin/MAX Viasonix Ltd.
K192607 09/20/2019 LiteWalk Viasonix Ltd.
K111416 05/20/2011 FALCON VIASONIX LTD.


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