The following data is part of a premarket notification filed by Directed Energy, Inc. with the FDA for Surgical Co2 Laser System #20/optical For Arthrosc.
Device ID | K854998 |
510k Number | K854998 |
Device Name: | SURGICAL CO2 LASER SYSTEM #20/OPTICAL FOR ARTHROSC |
Classification | Powered Laser Surgical Instrument |
Applicant | DIRECTED ENERGY, INC. 11661 SAN VICENTE BLVD. SUITE 203 Los Angeles, CA 90049 |
Contact | Edward Johansen |
Correspondent | Edward Johansen DIRECTED ENERGY, INC. 11661 SAN VICENTE BLVD. SUITE 203 Los Angeles, CA 90049 |
Product Code | GEX |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-12-12 |
Decision Date | 1986-05-02 |