ThermoNeuroModulation Device, TNM Device— 510(k) DEN170023
UnknownScion Neurostim, LLC
FDA 510(k) clearance DEN170023 for ThermoNeuroModulation Device, TNM Device, Unknown on 2018-03-26. Applicant: Scion Neurostim, LLC. Device class: 2.
Clearance details
- Applicant
- Scion Neurostim, LLC
- Product code
- Code QAR
- Device class
- Class 2
- Regulation
- 21 CFR 882.5893
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Raleigh, NC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.