Last synced on 14 November 2025 at 11:06 pm

GLIDE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131870
510(k) Type
Special
Applicant
HOME SKINOVATIONS LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/14/2013
Days to Decision
51 days
Submission Type
Summary

GLIDE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131870
510(k) Type
Special
Applicant
HOME SKINOVATIONS LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/14/2013
Days to Decision
51 days
Submission Type
Summary