FDA 510(k) Applications Submitted by W.A. RUBBERMATE CO., LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971200 | 04/01/1997 | W.A. | W.A. RUBBERMATE CO., LTD. |
| K021041 | 04/01/2002 | WA RUBBERMATE LATEX POWDER-FREE EXAM GLOVES | W.A. RUBBERMATE CO., LTD. |
| K110418 | 02/14/2011 | POWDER FREE NITRILE EXAMINATION GLOVES | W.A. RUBBERMATE CO., LTD. |
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