The following data is part of a premarket notification filed by Amd Lasers, Llc with the FDA for Picasso Laser System.
| Device ID | K083142 |
| 510k Number | K083142 |
| Device Name: | PICASSO LASER SYSTEM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | AMD LASERS, LLC 5 TIMBER LANE North Reading, MA 01864 |
| Contact | Maureen O'connell |
| Correspondent | Maureen O'connell AMD LASERS, LLC 5 TIMBER LANE North Reading, MA 01864 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-10-23 |
| Decision Date | 2009-03-13 |
| Summary: | summary |