K232977 is an FDA 510(k) clearance for the Biophotas Celluma CONTOUR. This device is classified as a Fat Reducing Low Level Laser (Class II - Special Controls, product code OLI).
Submitted by Biophotas, Inc. (Tustin, US). The FDA issued a Cleared decision on November 21, 2023, 61 days after receiving the submission on September 21, 2023.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.5400. Non-invasive Reduction In Fat Layer For Body Contouring.
| 510(k) Number | K232977 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 21, 2023 |
| Decision Date | November 21, 2023 |
| Days to Decision | 61 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OLI - Fat Reducing Low Level Laser |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.5400 |
| Definition | Non-invasive Reduction In Fat Layer For Body Contouring |