NeuroRPM— 510(k) K221772
Substantially EquivalentNew Touch Digital, Inc.
FDA 510(k) clearance K221772 for NeuroRPM, Substantially Equivalent on 2023-03-17. Applicant: New Touch Digital, Inc.. Device class: 2.
Clearance details
- Applicant
- New Touch Digital, Inc.
- Product code
- Code GYD
- Device class
- Class 2
- Regulation
- 21 CFR 882.1950
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Recent devices under product code GYD
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