The following data is part of a premarket notification filed by American Laser Medical with the FDA for Nuvolase 532 Cutaneous Laser System.
| Device ID | K990780 |
| 510k Number | K990780 |
| Device Name: | NUVOLASE 532 CUTANEOUS LASER SYSTEM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | AMERICAN LASER MEDICAL 1832 SOUTH 3850 WEST Salt Lake City, UT 84104 |
| Contact | Daniel Hoefer |
| Correspondent | Daniel Hoefer AMERICAN LASER MEDICAL 1832 SOUTH 3850 WEST Salt Lake City, UT 84104 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1999-03-09 |
| Decision Date | 1999-03-22 |
| Summary: | summary |