The following data is part of a premarket notification filed by Surgical Laser Technologies, Inc. with the FDA for Slt Clmd Contact Laser System (addit. Indication).
| Device ID | K890174 |
| 510k Number | K890174 |
| Device Name: | SLT CLMD CONTACT LASER SYSTEM (ADDIT. INDICATION) |
| Classification | Powered Laser Surgical Instrument |
| Applicant | SURGICAL LASER TECHNOLOGIES, INC. ONE GREAT VALLEY PKWY. Malvern, PA 19355 |
| Contact | Gifford, R.n. |
| Correspondent | Gifford, R.n. SURGICAL LASER TECHNOLOGIES, INC. ONE GREAT VALLEY PKWY. Malvern, PA 19355 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-01-09 |
| Decision Date | 1989-01-26 |