510(k) K130922
K130922 is an FDA 510(k) premarket notification submitted by Erchonia Medical, Inc. for the device "ERCHONIA VERJU LASER SYSTEM WITH MASSAGER". The FDA issued a decision of Substantially Equivalent on May 17, 2013. The device falls under product code OLI (Fat Reducing Low Level Laser), a Class II device regulated under 21 CFR 878.5400. Erchonia Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 17, 2013
- Date Received
- April 3, 2013
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fat Reducing Low Level Laser
- Device Class
- Class II
- Regulation Number
- 878.5400
- Review Panel
- SU
- Submission Type
Non-invasive reduction in fat layer for body contouring