GLIDE DEVICE— 510(k) K131870

Substantially Equivalent

Home Skinovations , Ltd.

FDA 510(k) clearance K131870 for GLIDE DEVICE, Substantially Equivalent on 2013-08-14. Applicant: Home Skinovations , Ltd..

Clearance details

Applicant: Home Skinovations , Ltd.
Product code: Code OHT
Advisory panel: General, Plastic Surgery
Date received: 2013-06-24
Decision date: 2013-08-14
Decision: Substantially Equivalent
Clearance type: Special
Location: Kfar Saba, IL

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