FDA 510(k) Applications Submitted by JDA (TIANJIN) PLASTIC RUBBER CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030529 | 02/19/2003 | LEGEND (BRAND) NITRILE POWDER-FREE PATIENT EXAMINATION GLOVE | JDA (TIANJIN) PLASTIC RUBBER CO., LTD. |
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