FDA 510(k) Applications Submitted by Jie Xia
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K201076 | 04/22/2020 | Anchor Dual Lumen Guidewire Catheter | Aqure Medical, Inc. |
| K220245 | 01/28/2022 | Pocket Fetal Doppler (Models CONTEC10C and CONTEC10CL) | Contec Medical Systems Co., Ltd. |
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