The following data is part of a premarket notification filed by Laserscope with the FDA for Ktp/532 & Ktp/yag.
| Device ID | K913990 |
| 510k Number | K913990 |
| Device Name: | KTP/532 & KTP/YAG |
| Classification | Powered Laser Surgical Instrument |
| Applicant | LASERSCOPE 3052 ORCHARD DR. San Jose, CA 95134 -2011 |
| Contact | Donna Page |
| Correspondent | Donna Page LASERSCOPE 3052 ORCHARD DR. San Jose, CA 95134 -2011 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-09-05 |
| Decision Date | 1992-09-02 |