K133473 is an FDA 510(k) clearance for the ILUMINAGE SKIN SMOOTHING LASER, a Light Based Over The Counter Wrinkle Reduction (Class II — Special Controls, product code OHS), submitted by Cynosure, Inc. (Wesford, US). The FDA issued a Cleared decision on January 15, 2014, 64 days after receiving the submission on November 12, 2013. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K133473 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 12, 2013 |
| Decision Date | January 15, 2014 |
| Days to Decision | 64 days |
| Submission Type | Special |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OHS — Light Based Over The Counter Wrinkle Reduction |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | Use Of Light Based Treatment To Reduce Wrinkles On The Body In General Or Specific Anatomical Locations Depending On The Information Provided. |