The following data is part of a premarket notification filed by Cynosure, Inc. with the FDA for Cynosure Dioderm.
| Device ID | K992765 |
| 510k Number | K992765 |
| Device Name: | CYNOSURE DIODERM |
| Classification | Powered Laser Surgical Instrument |
| 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 | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-08-17 |
| Decision Date | 1999-09-08 |