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 |