FDA 510(k) Applications Submitted by FORTIFIER INTERNATIONAL CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K041400 | 05/26/2004 | FORTIFIER DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL LF-01 | FORTIFIER INTERNATIONAL CO., LTD. |
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