Neurosteer EEG Recorder— 510(k) K221563
Substantially EquivalentNeurosteer, Inc.
FDA 510(k) clearance K221563 for Neurosteer EEG Recorder, Substantially Equivalent on 2022-10-24. Applicant: Neurosteer, Inc.. Device class: 2.
Clearance details
- Applicant
- Neurosteer, Inc.
- Product code
- Code OMC
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Recent devices under product code OMC
view allData sourced from openFDA. This site is unofficial and independent of the FDA.