FDA 510(k) Applications Submitted by Acare Technology Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111617 | 06/10/2011 | PULSE OXIMETER MODEL AB-F1/AH-S1/AH-M1 | ACARE TECHNOLOGY CO., LTD. |
| K182950 | 10/23/2018 | Acare Suction Unit | Acare Technology Co., Ltd. |
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