Hangzhou Jimushi Meditech Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest Approval2023-04-05
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K222677 | Intermittent nelaton catheter for single use | EZD | 2023-04-05 | View |
| 510(k) | K200134 | Jimushi Sterile Urethral Catheter for single use | GBM | 2020-06-01 | View |
No matching devices.