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#
- 3013376016
- 3009217531
- 3006561161
- 3027339877
- 3005064943
- 9611503
- 3006639944
- 8010312
- 1721504
- 3003687489
- 2087572
- 3012995405
- 1320894
- 3008843439
- 1222780
- 8030967
- 3015153469
- 3014479313
- 3007593903
- 3006807694
- 2183785
- 3012616488
- 3026606306
- 2433012
- 1221934
- 3014656892
- 3005528784
- 3008747667
- 3009763019
- 3011050570
- 9680660
- 3027242374
- 3012447612
- 3004361445
- 3007748817
- 3031916226
- 3013602304
- 3002808022
- 3015976667
- 2528981
- 3014980461
- 3015895045
- 3016087306
- 3015531529
- 3011120183
- 3008849319
- 3002806603
- 3015460875
- 3010739934
- 3020163307
- 3010132111
- 2219920
- 9613793
- 3029916132
- 3011221476
- 3015449142
- 3004044817
- 3018094310
- 9680952
- 1043214
- 3010601992
- 3009051888
- 3012263546
- 1061927
- 3032109
- 3007867778
- 3010805941
- 3016020790
- 3020968442
- 3048141561
- 3006638824
- 8040510
- 3003542872
- 3010493171
- 3011683674
- 3011989678
- 3012259264
- 1225492
- 3010188783
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#
Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links Follow FDA En Español Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products FDA Home Medical Devices Databases