The following data is part of a premarket notification filed by Cynosure, Inc. with the FDA for Cynosurea Eclilite And Eclilite U.
| Device ID | K050080 |
| 510k Number | K050080 |
| Device Name: | CYNOSUREA ECLILITE AND ECLILITE U |
| Classification | Light, Ultraviolet, Dermatological |
| Applicant | CYNOSURE, INC. 10 ELIZABETH DR. Chelmsford, MA 01824 |
| Contact | George Cho |
| Correspondent | George Cho CYNOSURE, INC. 10 ELIZABETH DR. Chelmsford, MA 01824 |
| Product Code | FTC |
| CFR Regulation Number | 878.4630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2005-01-13 |
| Decision Date | 2005-05-05 |
| Summary: | summary |