INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE— 510(k) K070217
Substantially EquivalentNeuro Resource Group, Inc.
FDA 510(k) clearance K070217 for INTERX 1000/DERMA 200 STIMULATOR FOR COSMETIC USE, Substantially Equivalent on 2008-04-04. Applicant: Neuro Resource Group, Inc.. Device class: 2.
Clearance details
- Applicant
- Neuro Resource Group, Inc.
- Product code
- Code NFO
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plano, TX, US
Recent devices under product code NFO
view allMore clearances from Neuro Resource Group, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.