GLIDE DEVICE— 510(k) K141242
Substantially EquivalentHome Skinovations , Ltd.
FDA 510(k) clearance K141242 for GLIDE DEVICE, Substantially Equivalent on 2014-10-17. Applicant: Home Skinovations , Ltd..
Clearance details
- Applicant
- Home Skinovations , Ltd.
- Product code
- Code OHT
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kfar Saba, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.