Zhejiang Curaway Medical Technology Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K244018 | Disposable Biopsy Needle | July 22, 2025 |
| K242322 | Bone Marrow Biopsy Needle | January 24, 2025 |
| K241793 | Automatic Core Biopsy Instrument/ Semi-Automatic Core Biopsy Instrument/ Disposable Coaxial Biopsy N | January 24, 2025 |
| K240758 | Radiofrequency Generator System, Cura RF Electrode | December 11, 2024 |
| K232505 | Endovenous Radiofrequency Generator, Endovenous Radiofrequency Catheter | May 30, 2024 |
| K222001 | Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe | June 8, 2023 |