The following data is part of a premarket notification filed by Quantel Medical with the FDA for Viridis Derma Laser.
| Device ID | K020071 |
| 510k Number | K020071 |
| Device Name: | VIRIDIS DERMA LASER |
| Classification | Powered Laser Surgical Instrument |
| Applicant | QUANTEL MEDICAL 342 SUNSET BAY RD. Hot Springs, AR 71913 |
| Contact | Roger W Barnes |
| Correspondent | Roger W Barnes QUANTEL MEDICAL 342 SUNSET BAY RD. Hot Springs, AR 71913 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-01-09 |
| Decision Date | 2002-04-05 |
| Summary: | summary |