Bain Medical Equipment (Guangzhou) 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 |
|---|
| K240164 | NovaLine SP-C35 Transducer Protector (956007) | June 28, 2024 |
| K213015 | DORA Disposable A.V. Fistula Needle Sets | April 8, 2022 |
| K201866 | NovaLine Tubing Sets for Hemodialysis | March 10, 2021 |
| K203524 | Surgical Masks | February 25, 2021 |
| K163025 | DORA Disposable A.V. Fistula Needle Sets | July 20, 2017 |
| K161582 | DORA Tubing Sets for Hemodialysis | June 16, 2017 |