FDA 510(k) Applications Submitted by Han Wang
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K160320 | 02/05/2016 | Premier | Shandong Weigao Orthopaedic Device Co., Ltd |
| K170861 | 03/23/2017 | Premier | Shandong Weigao Orthopaedic Device Co., Ltd. |
| K112449 | 08/25/2011 | QUIKRESPONSE ONE STEP MIDSTREAM EARLY PREGRANCY TEST | Tianjin New Bay Bioresearch Co., Ltd. |
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