Asahi Polyslider Co., Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2022-11-02
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222084 | OneTouch Delica Safety, HemoCue Safety Lancet, Assure Lance and Assure Lance Plus, Capiject Safety Lancet, Heel Lancet Newborn, Heel Lancet Preemie | FMK | 2022-11-02 | View |
| 510(k) | K221546 | OneTouch Delica Plus Lancing System | QRL | 2022-08-23 | View |
No matching devices.