FDA 510(k) Applications Submitted by LPL (HUI ZHOU) GLOVE CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K111598 | 06/08/2011 | POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVE | LPL (HUI ZHOU) GLOVE CO., LTD. |
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