REJUVENIQUE MODEL #RJV10— 510(k) K011935
Substantially EquivalentSalton, Inc.
FDA 510(k) clearance K011935 for REJUVENIQUE MODEL #RJV10, Substantially Equivalent on 2001-08-08. Applicant: Salton, Inc.. Device class: 2.
Clearance details
- Applicant
- Salton, 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
- Washington, DC, US
Recent devices under product code NFO
view allMore clearances from Salton, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.