FDA 510(k) Applications Submitted by HANDSAFE PRODUCTS SDN. BHD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960386 | 01/26/1996 | HANDSAFE | HANDSAFE PRODUCTS SDN. BHD. |
| K000913 | 03/22/2000 | POWDER FREE LATEX PATIENT EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS) | HANDSAFE PRODUCTS SDN. BHD. |
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