The following data is part of a premarket notification filed by Lutronic Corporation with the FDA for Mosaic Eco2 Laser System.
Device ID | K080496 |
510k Number | K080496 |
Device Name: | MOSAIC ECO2 LASER SYSTEM |
Classification | Powered Laser Surgical Instrument |
Applicant | LUTRONIC CORPORATION 5 TIMBER LANE North Reading, MA 01864 |
Contact | Maureen O'connell |
Correspondent | Maureen O'connell LUTRONIC CORPORATION 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 | 2008-02-22 |
Decision Date | 2008-07-07 |
Summary: | summary |