FDA 510(k) Applications Submitted by PREMIER PATHWAY SDN. BHD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K001327 | 04/26/2000 | POWDERED LATEX EXAM GLOVES, PROTEIN LABELING (150 MICROGRAM OR LESS) | PREMIER PATHWAY SDN. BHD. |
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