The following data is part of a premarket notification filed by New Star Lasers, Inc. with the FDA for 6 Watt Holmium Laser System.
Device ID | K952489 |
510k Number | K952489 |
Device Name: | 6 WATT HOLMIUM LASER SYSTEM |
Classification | Powered Laser Surgical Instrument |
Applicant | NEW STAR LASERS, INC. 1000 BURNETT AVE. SUITE 450 Concord, CA 94520 |
Contact | David W Schlerf |
Correspondent | David W Schlerf NEW STAR LASERS, INC. 1000 BURNETT AVE. SUITE 450 Concord, CA 94520 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-05-30 |
Decision Date | 1996-01-22 |