The following data is part of a premarket notification filed by Continuum Electro-optics, Inc. with the FDA for Multilite Erbium:yag Surgical Laser System.
Device ID | K933057 |
510k Number | K933057 |
Device Name: | MULTILITE ERBIUM:YAG SURGICAL LASER SYSTEM |
Classification | Powered Laser Surgical Instrument |
Applicant | CONTINUUM ELECTRO-OPTICS, INC. 3150 CENTRAL EXPRESSWAY Santa Clara, CA 95051 |
Contact | Gerry W Garcia |
Correspondent | Gerry W Garcia CONTINUUM ELECTRO-OPTICS, INC. 3150 CENTRAL EXPRESSWAY Santa Clara, CA 95051 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-06-22 |
Decision Date | 1994-11-01 |