Last synced on 14 November 2025 at 11:06 pm

LiteWalk

Page Type
Cleared 510(K)
510(k) Number
K192607
510(k) Type
Traditional
Applicant
Viasonix Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/19/2019
Days to Decision
90 days
Submission Type
Summary

LiteWalk

Page Type
Cleared 510(K)
510(k) Number
K192607
510(k) Type
Traditional
Applicant
Viasonix Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
12/19/2019
Days to Decision
90 days
Submission Type
Summary