510(k) K214058
- Device
- Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer
- Applicant
- ConMed Corporation
- 510(k) number
- K214058
- Product code
- KNS
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2022-08-26
- Date received
- 2021-12-27
- Regulation
- 876.4300
- Classification name
- Unit, Electrosurgical, Endoscopic (with Or Without Accessories)
- Medical specialty
- Gastroenterology/Urology
- Review panel
- General & Plastic Surgery
- Device class
- 2
- Clearance type
- Traditional
- Statement or summary
- Summary
- Third party reviewed
- No
Applicant Contact#
- Contact
- Kavita Amin
- Address
- 525 French Rd. Utica NY US 13502 13502
FDA Registration Numbers#
- 3003935342
- 1222140
- 3015974593
- 3026606306
- 3005075853
- 3001431138
- 3010687973
- 3019569846
- 3007421149
- 1418975
- 3012453745
- 9614279
- 3009736547
- 1319639
- 3004940677
- 3010885402
- 3014004349
- 3029754081
- 3011683674
- 1223422
- 1222993
- 3010164891
- 3007748793
- 3010361165
- 8040510
- 3005646850
- 3010684280
- 8040537
- 3016678045
- 1421879
- 1423537
- 3000268902
- 3009183442
- 3006017180
- 9610617
- 3003767927
- 3012783431
- 3011024991
- 3036773433
- 3008264458
- 3012818475
- 3012616488
- 2521453
- 9710058
- 3030412764
- 1412854
- 2133936
- 3003418325
- 3011063460
- 2084346
- 3003072803
- 3012428212
- 3013700547
- 2183613
- 8030607
- 3016813690
- 3004837686
- 3002808022
- 3011559089
- 3003687489
- 3042272797
- 8010418
- 3017892510
- 3045753434
- 3013176080
- 3002808227
- 3013789508
- 2087572
- 3013820501
- 1061124
- 3015151147
- 3030626857
- 3006950086
- 3015286855
- 3006897899
- 3016555232
- 3016607092
- 8010298
- 3042940623
Source Documents#
Other 510(k) Records For Product Code KNS #
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K262460 | Rezum System | Boston Scientific | 2026-09-03 |
| K260962 | Sphincterotome | Taewoong Medical Co., Ltd. | 2026-05-21 |
| K252388 | Vanquish Water Vapor Ablation Device | Francis Medical, Inc. | 2025-11-26 |
| K252889 | Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M) | Olympus Medical Systems Corporation | 2025-11-25 |
| K250945 | Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series) | Olympus Medical Systems Corp. | 2025-10-17 |
| K250351 | Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U) | Olympus Medical Systems Corporation | 2025-10-10 |
| K251104 | SureTome™ SW Sphincterotome with DomeTip | Wilson-Cook Medical | 2025-09-29 |
| K251226 | Aqua Medical RF Vapor Ablation System | Aqua Medical, Inc. | 2025-08-08 |
| K250584 | Rezum System | Boston Scientific Corporation | 2025-06-11 |
| K242774 | SpydrBlade Flex Instrument (PRD-RG1-001) | Creo Medical, Ltd. | 2025-06-06 |
| K241855 | SB Knife Jr2 (MD-47702 and MD-47702L) | Sb-Kawasumi Laboratories, Inc. | 2025-03-26 |
| K242192 | Disposable Sphincterotome | Beijing Zksk Technology Co., Ltd. | 2025-02-06 |
| K243568 | Teslatome Bipolar Sphincterotome; Tesla BiCord Active Cord | Wilson-Cook Medical, Inc. | 2025-01-17 |
| K241271 | Aqua Medical RF Vapor Ablation System | Aqua Medical, Inc. | 2024-12-12 |
| K242061 | Reusable Interface Cable 1.5 m (PRD-IFC-002) | Creo Medical, Ltd. | 2024-08-15 |
Legacy Summary#
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FDA Review#
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