The following data is part of a premarket notification filed by Candela Corp. with the FDA for Candela Gentleyag Family Of Laser Systems.
| Device ID | K033172 |
| 510k Number | K033172 |
| Device Name: | CANDELA GENTLEYAG FAMILY OF LASER SYSTEMS |
| Classification | Powered Laser Surgical Instrument |
| Applicant | CANDELA CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Contact | Lorraine Calzetta-patrovic |
| Correspondent | Lorraine Calzetta-patrovic 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 | 2003-09-30 |
| Decision Date | 2003-10-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817495024639 | K033172 | 000 |