The following data is part of a premarket notification filed by Directed Energy, Inc. with the FDA for Model 20-c With An Sa-20b/u Opt. Attach. Hemorrho..
Device ID | K871029 |
510k Number | K871029 |
Device Name: | MODEL 20-C WITH AN SA-20B/U OPT. ATTACH. HEMORRHO. |
Classification | Laser For Gastro-urology Use |
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 | LNK |
CFR Regulation Number | 878.4810 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-16 |
Decision Date | 1987-05-18 |