Canady Helios Cold Plasma XL-1000CP Ablation System (XL-1000CPSYS)
FDA 510(k) K240297 · Us Medical Innovations, LLC
510(k) numberK240297
Submission
- Device name
- Canady Helios Cold Plasma XL-1000CP Ablation System (XL-1000CPSYS)
- Applicant
- Us Medical Innovations, LLC
Tacoma Park, MD, US - Received
- February 1, 2024
- Decision date
- May 3, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- OAB – Low Energy Direct Current Thermal Ablation System
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.4400
- Specialty
- General, Plastic Surgery
Ablation of soft tissue
Other 510(k)s with product code OAB
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K253846 | Steep Pulse Ablation Instrument (including Disposable Sterile Steep Pulse Probe)…OAB · Traditional | Hangzhou Ruidi Biotechnology , Ltd. | 08/12/2026SE |
| K253826 | Aliya® EX System; Aliya® EX Generator; Aliya® Needle; Aliya® Electrode; INUMI Flex NeedleOAB · Traditional | Galvanize Therapeutics, Inc. | 05/07/2026SE |
| K253198 | NanoKnife Generator (H78720300351US0)OAB · Traditional | Angiodynamics | 03/24/2026SE |
| K242687 | NanoKnife Generator (H78720300301US0); NanoKnife Single Electrode Activation Probe, 15…OAB · Traditional | AngioDynamics, Inc. | 12/06/2024SE |
| K240376 | Electroporation System (N3000)OAB · Traditional | Surgnova Healthcare Technologies (Zhejiang) Co.… | 10/04/2024SE |
| K233884 | INUMI Flex NeedleOAB · Traditional | Galvanize Therapeutics, Inc. | 05/22/2024SE |
| K222001 | Irreversible Electroporation Ablation Generator, Irreversible Electroporation ProbeOAB · Traditional | Zhejiang Curaway Medical Technology Co., Ltd. | 06/08/2023SE |
| K212871 | Aliya(TM) System, Aliya(TM) Generator, Aliya(TM) Needle, Aliya(TM) ElectrodeOAB · Traditional | Galvanize Therapeutics, Inc. | 06/17/2022SE |
| K183385 | NanoKnife SystemOAB · Traditional | Angiodynamics | 06/18/2019SE |
| K150089 | NanoKnife SystemOAB · Traditional | AngioDynamics, Inc. | 06/18/2015SE |
More from AngioDynamics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K212736 | Canady Flex RoboWristGCJ · Traditional | 11/22/2022SE |
| K192124 | Canady Plasma SMART XL-1000 Electrosurgical Generator with AccessoriesGEI · Special | 11/21/2019SE |
| K113500 | Canady Vieira Hybrid Plasma ScalpelGEI · Traditional | 12/09/2011SE |
| K100669 | Canady Plasma Electrosurgical Unit Series with Accessory Probes and BladesGEI · Traditional | 04/06/2011SE |
Questions and answers
When was Canady Helios Cold Plasma XL-1000CP Ablation System (XL-1000CPSYS) cleared by the FDA?
Canady Helios Cold Plasma XL-1000CP Ablation System (XL-1000CPSYS) (K240297) received a 510(k) decision of Substantially Equivalent on May 3, 2024, 92 days after the submission was received.
What is the product code of K240297?
The FDA product code is OAB – Low Energy Direct Current Thermal Ablation System, a Class II (moderate risk) device regulated under 21 CFR 878.4400.