The following data is part of a premarket notification filed by Cooper Lasersonics, Inc. with the FDA for Cusa System 200 Macro-dissector.
Device ID | K864983 |
510k Number | K864983 |
Device Name: | CUSA SYSTEM 200 MACRO-DISSECTOR |
Classification | Instrument, Ultrasonic Surgical |
Applicant | COOPER LASERSONICS, INC. 3420 Central Expressway Santa Clara, CA 95051 |
Contact | Charles L Rose |
Correspondent | Charles L Rose COOPER LASERSONICS, INC. 3420 Central Expressway Santa Clara, CA 95051 |
Product Code | LFL |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-22 |
Decision Date | 1987-06-23 |