The following data is part of a premarket notification filed by Valleylab, Inc. with the FDA for Cv720-727-000, Microtip And Flue Pak.
Device ID | K933239 |
510k Number | K933239 |
Device Name: | CV720-727-000, MICROTIP AND FLUE PAK |
Classification | Instrument, Ultrasonic Surgical |
Applicant | VALLEYLAB, INC. 5920 LONGBOW DR. Boulder, CO 80301 |
Contact | Lynne Leonard |
Correspondent | Lynne Leonard 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 | 1993-07-02 |
Decision Date | 1993-10-12 |