The following data is part of a premarket notification filed by Conmed Corporation with the FDA for Beamer Aveo Electrosurgical Generator, Beamer Aveo Argon Module, Beamer Aveo Cart, Beamer Aveo Wired Foot Pedal, Beamer Aveo Argon Pressure Reducer.
| Device ID | K214058 |
| 510k Number | K214058 |
| Device Name: | Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer |
| Classification | Unit, Electrosurgical, Endoscopic (with Or Without Accessories) |
| Applicant | ConMed Corporation 525 French Road Utica, NY 13502 |
| Contact | Kavita Amin |
| Correspondent | Kavita Amin ConMed Corporation 525 French Road Utica, NY 13502 |
| Product Code | KNS |
| CFR Regulation Number | 876.4300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2021-12-27 |
| Decision Date | 2022-08-26 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10845854082836 | K214058 | 000 |
| 10845854082829 | K214058 | 000 |
| 10845854082812 | K214058 | 000 |
| 10845854082515 | K214058 | 000 |
| 10845854082379 | K214058 | 000 |
| 10845854081501 | K214058 | 000 |
| 10845854081495 | K214058 | 000 |