FDA 510(k) Applications Submitted by EVERGRADE HEALTHCARE PRODUCTS SDN BHD
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K973664 | 09/25/1997 | LATEX EXAM GLOVE, POWDER-FREE W/PROTEIN & HYPOALLERGENIC LABELING | EVERGRADE HEALTHCARE PRODUCTS SDN BHD |
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