FDA 510(k) Applications Submitted by Weipeng (Suzhou) Medical Devices Co., Ltd.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K202119 | 07/30/2020 | AcuSee AS-P1000 System | Weipeng (Suzhou) Medical Devices Co., Ltd. |
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