The following data is part of a premarket notification filed by Candela Corp. with the FDA for Candela Gentlelase Gl Dermatological Laser.
| Device ID | K994260 |
| 510k Number | K994260 |
| Device Name: | CANDELA GENTLELASE GL DERMATOLOGICAL LASER |
| Classification | Powered Laser Surgical Instrument |
| Applicant | CANDELA CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Contact | Jay Caplan |
| Correspondent | Jay Caplan CANDELA CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-12-17 |
| Decision Date | 2000-05-26 |
| Summary: | summary |