SMARTVERTIGO Vestibular Assessment System— 510(k) K260566
Substantially EquivalentVertigoDx, Inc.
FDA 510(k) clearance K260566 for SMARTVERTIGO Vestibular Assessment System, Substantially Equivalent on 2026-07-30. Applicant: VertigoDx, Inc.. Device class: 2.
Clearance details
- Applicant
- VertigoDx, Inc.
- Product code
- Code GWN
- Device class
- Class 2
- Regulation
- 21 CFR 882.1460
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wilmington, DE, US
Recent devices under product code GWN
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