The following data is part of a premarket notification filed by Laser Photonics, Inc. with the FDA for Laserphotonics Ml300 Stonelaser Alexandrite Lith..
Device ID | K920334 |
510k Number | K920334 |
Device Name: | LASERPHOTONICS ML300 STONELASER ALEXANDRITE LITH. |
Classification | Powered Laser Surgical Instrument |
Applicant | LASER PHOTONICS, INC. 12351 RESEARCH PKWY. Orlando, FL 32826 |
Contact | Robert J Anselmo |
Correspondent | Robert J 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 | 1992-01-27 |
Decision Date | 1993-03-31 |