Neurosplint— 510(k) K143458
Substantially EquivalentNeurospectrum, LLC
FDA 510(k) clearance K143458 for Neurosplint, Substantially Equivalent on 2015-08-13. Applicant: Neurospectrum, LLC. Device class: 1.
Clearance details
- Applicant
- Neurospectrum, LLC
- Product code
- Code IQI
- Device class
- Class 1
- Regulation
- 21 CFR 890.3475
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Rancho Mirage, CA, US
Recent devices under product code IQI
view allData sourced from openFDA. This site is unofficial and independent of the FDA.