FDA 510(k) Applications Submitted by TK LOH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K062917 | 09/28/2006 | STERILE AND NON-STERILE POWDER-FREE LATEX PATIENT EXAMINATION GLOVE, WITH EXTRACTABLE PROTEIN CONTENT LABELING CLAIM (50 | WEAR SAFE MALAYSIA SDN. BHD. |
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