Submission Details
| 510(k) Number | K140527 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 04, 2014 |
| Decision Date | July 31, 2014 |
| Days to Decision | 149 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
K140527 is an FDA 510(k) clearance for the SENSILIGHT MINI, a Light Based Over-the-counter Hair Removal (Class II — Special Controls, product code OHT), submitted by El Global Trade, Ltd. (Netanya, IL). The FDA issued a Cleared decision on July 31, 2014, 149 days after receiving the submission on March 4, 2014. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K140527 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | March 04, 2014 |
| Decision Date | July 31, 2014 |
| Days to Decision | 149 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | OHT — Light Based Over-the-counter Hair Removal |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | Over-the-counter Device Uses Thermal Energy To Kill Hair Follicles For Hair Removal. |