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Suzhou Haishen Medical Device Associates Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K232888 | Disposable Laryngeal Electrodes | December 21, 2023 |
| K232581 | Medical Disposable Sterile Needle Electrode | December 4, 2023 |