The following data is part of a premarket notification filed by Covidien Llc with the FDA for Valleylab Fx8 Electrosurgical Platform.
| Device ID | K172757 |
| 510k Number | K172757 |
| Device Name: | Valleylab FX8 Electrosurgical Platform |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | Covidien Llc 5920 Longbow Drive Boulder, CO 80301 |
| Contact | Sharon Mcdermott |
| Correspondent | Sharon Mcdermott Covidien Llc 5920 Longbow Drive Boulder, CO 80301 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-09-13 |
| Decision Date | 2017-11-02 |
| Summary: | summary |