FDA 510(k) Applications Submitted by WENZHOU BOKANG INSTRUMENTS CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111141 | 04/22/2011 | BOKANG SEMI-AUTO / AUTOMATIC / WRIST DIGITAL BLOOD PRESSURE MONITOR | WENZHOU BOKANG INSTRUMENTS CO., LTD. |
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