The following data is part of a premarket notification filed by Candela Laser Corp. with the FDA for Mdl-2000 Lasertripter.
| Device ID | K901723 |
| 510k Number | K901723 |
| Device Name: | MDL-2000 LASERTRIPTER |
| Classification | Laser For Gastro-urology Use |
| Applicant | CANDELA LASER CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Contact | George Cho |
| Correspondent | George Cho CANDELA LASER CORP. 530 BOSTON POST RD. Wayland, MA 01778 |
| Product Code | LNK |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-04-16 |
| Decision Date | 1990-07-13 |