The following data is part of a premarket notification filed by Candela Laser Corp. with the FDA for Candela Q-switched Alexandrite Lasers.
| Device ID | K955662 |
| 510k Number | K955662 |
| Device Name: | CANDELA Q-SWITCHED ALEXANDRITE LASERS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | CANDELA LASER CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Contact | Jay Caplan |
| Correspondent | Jay Caplan CANDELA LASER 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 | 1995-12-12 |
| Decision Date | 1996-06-14 |
| Summary: | summary |