Last synced on 14 November 2025 at 11:06 pm

HX Device

Page Type
Cleared 510(K)
510(k) Number
K173919
510(k) Type
Traditional
Applicant
Human Extension Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2018
Days to Decision
88 days
Submission Type
Summary

HX Device

Page Type
Cleared 510(K)
510(k) Number
K173919
510(k) Type
Traditional
Applicant
Human Extension Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
3/20/2018
Days to Decision
88 days
Submission Type
Summary