LOUSEBUSTER— 510(k) K093144
Substantially EquivalentLarada Sciences
FDA 510(k) clearance K093144 for LOUSEBUSTER, Substantially Equivalent on 2009-12-16. Applicant: Larada Sciences. Device class: 1.
Clearance details
- Applicant
- Larada Sciences
- Product code
- Code LJL
- Device class
- Class 1
- Regulation
- 21 CFR 880.5960
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Salt Lake City, UT, US
Recent devices under product code LJL
view allData sourced from openFDA. This site is unofficial and independent of the FDA.