FDA 510(k) Applications Submitted by KOJI KOBO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080177 | 01/24/2008 | WRIST BLOOD PRESSURE MONITOR, MODEL WS-1100/WS-1100PV | NIHON SEIMITSU SOKKI CO., LTD. |
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