The following data is part of a premarket notification filed by Laser Photonics, Inc. with the FDA for Multilase 60.
| Device ID | K904229 |
| 510k Number | K904229 |
| Device Name: | MULTILASE 60 |
| Classification | Powered Laser Surgical Instrument |
| Applicant | LASER PHOTONICS, INC. 12351 RESEARCH PKWY. Orlando, FL 32826 |
| Contact | Robert Anselmo |
| Correspondent | Robert Anselmo LASER PHOTONICS, INC. 12351 RESEARCH PKWY. Orlando, FL 32826 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-09-13 |
| Decision Date | 1990-12-12 |