The following data is part of a premarket notification filed by Heraeus Lasersonics, Inc. with the FDA for Co2 Laser System & Arthoguide Co2 Laser Fiber Del..
| Device ID | K883488 |
| 510k Number | K883488 |
| Device Name: | CO2 LASER SYSTEM & ARTHOGUIDE CO2 LASER FIBER DEL. |
| Classification | Powered Laser Surgical Instrument |
| Applicant | HERAEUS LASERSONICS, INC. 3420 CENTRAL EXPRESSWAY P.O. BOX 58005 Santa Clara, CA 95051 -0793 |
| Contact | Charles L Rose |
| Correspondent | Charles L Rose HERAEUS LASERSONICS, INC. 3420 CENTRAL EXPRESSWAY P.O. BOX 58005 Santa Clara, CA 95051 -0793 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-08-16 |
| Decision Date | 1988-12-19 |