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GLIDE DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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