K222265 is an FDA 510(k) clearance for the Diosculpt. This device is classified as a Laser For Disruption Of Adipocyte Cells For Aesthetic Use (Class II - Special Controls, product code PKT).
Submitted by Shanghai Wonderful Opto-Electrics Tech.Co.,Ltd (Shanghai, CN). The FDA issued a Cleared decision on September 23, 2022, 57 days after receiving the submission on July 28, 2022.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.5400. Laser Intended For The Disruption Of Adipocyte Cells Indicated For Body Contouring Or Reduction In Circumference Of Body Areas..
| 510(k) Number | K222265 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | July 28, 2022 |
| Decision Date | September 23, 2022 |
| Days to Decision | 57 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | PKT - Laser For Disruption Of Adipocyte Cells For Aesthetic Use |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.5400 |
| Definition | Laser Intended For The Disruption Of Adipocyte Cells Indicated For Body Contouring Or Reduction In Circumference Of Body Areas. |