K131362 is an FDA 510(k) clearance for the INMODE WMBODY DEVICE. This device is classified as a Massager, Vacuum, Light Induced Heating (Class II - Special Controls, product code NUV).
Submitted by Inmode MD , Ltd. (Kfar Saba, IL). The FDA issued a Cleared decision on October 8, 2013, 148 days after receiving the submission on May 13, 2013.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4810. The Device Is Intended To Temporarily Alter The Appearance Of Cellulite.
| 510(k) Number | K131362 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 13, 2013 |
| Decision Date | October 08, 2013 |
| Days to Decision | 148 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | NUV - Massager, Vacuum, Light Induced Heating |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | The Device Is Intended To Temporarily Alter The Appearance Of Cellulite |