InMode System with vTone Applicator— 510(k) K200293
Substantially EquivalentInMode , Ltd.
FDA 510(k) clearance K200293 for InMode System with vTone Applicator, Substantially Equivalent on 2020-05-05. Applicant: InMode , Ltd.. Device class: 2.
Clearance details
- Applicant
- InMode , Ltd.
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Yokneam, IL
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More clearances from InMode , Ltd.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.