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Alton (Shanghai) Medical Instruments 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 |
|---|
| K243039 | Ureteral Stents (AF-D series) | June 18, 2025 |
| K242635 | Endoscopic Distal Attachment (AF-D series) | May 30, 2025 |
| K241679 | Disposable Cytology Brush (AF series) | March 4, 2025 |
| K241285 | Disposable Endoscope Valves Set (AF series) | October 1, 2024 |
| K231633 | Disposable Hemoclip (AF series) | January 11, 2024 |
| K230925 | Disposable Injection Needle AF series | September 27, 2023 |