FDA 510(k) Applications Submitted by DEHAI (SHANDONG) MEDICAL GLOVES, CO., LTD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K123869 | 12/17/2012 | POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES | DEHAI (SHANDONG) MEDICAL GLOVES, CO., LTD |
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