Suzhou Leapmed Healthcare Corporation
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K212819 | Disposable Biopsy Refill Needle | July 6, 2022 |
| K212820 | Disposable Semi Automatic Biopsy Instrument | July 6, 2022 |
| K212822 | Disposable Coaxial Biopsy Needle | July 6, 2022 |
| K212284 | Disposable Automatic Core Biopsy Instrument | November 10, 2021 |