The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Cusa System 200c And 200t Ultrasonic Aspirator.
Device ID | K921251 |
510k Number | K921251 |
Device Name: | CUSA SYSTEM 200C AND 200T ULTRASONIC ASPIRATOR |
Classification | Instrument, Ultrasonic Surgical |
Applicant | VALLEYLAB, INC. 5920 LONGBOW DR. Boulder, CO 80301 |
Contact | Peggy Walline |
Correspondent | Peggy Walline VALLEYLAB, INC. 5920 LONGBOW DR. Boulder, CO 80301 |
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 | 1992-03-16 |
Decision Date | 1992-06-12 |