The following data is part of a premarket notification filed by Surgilase, Inc. with the FDA for Surgilase Sl 50/60 Gold Surgical Laser System.
| Device ID | K904203 |
| 510k Number | K904203 |
| Device Name: | SURGILASE SL 50/60 GOLD SURGICAL LASER SYSTEM |
| Classification | Powered Laser Surgical Instrument |
| Applicant | SURGILASE, INC. I-95 CORPORATE PARK 33 PLAN WAY Warwick, RI 02866 |
| Contact | Timothy J Shea |
| Correspondent | Timothy J Shea SURGILASE, INC. I-95 CORPORATE PARK 33 PLAN WAY Warwick, RI 02866 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-09-12 |
| Decision Date | 1990-12-07 |