The following data is part of a premarket notification filed by Candela Corp. with the FDA for Candela Gentlemax Family Of Laser Systems.
| Device ID | K133283 |
| 510k Number | K133283 |
| Device Name: | CANDELA GENTLEMAX FAMILY OF LASER SYSTEMS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | CANDELA CORP. 530 BOSTON POST ROAD Wayland, MA 01778 |
| Contact | Sam Wade |
| Correspondent | Sam Wade CANDELA CORP. 530 BOSTON POST ROAD Wayland, MA 01778 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-10-25 |
| Decision Date | 2013-12-26 |
| Summary: | summary |