FDA 510(k) Applications Submitted by GENTEEL TECHNOLOGY CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K022926 | 08/04/2002 | GENTEEL WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL BP-100 | GENTEEL TECHNOLOGY CO., LTD. |
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