FDA 510(k) Applications Submitted by SHANDONG YUYUAN LATEX GLOVES COMPANY LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K072639 | 09/18/2007 | YUYUAN LATEX EXAMINATION GLOVE, POWDERED | SHANDONG YUYUAN LATEX GLOVES COMPANY LTD. |
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