FDA 510(k) Applications Submitted by OMNI INTL., INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K984064 | 11/16/1998 | OMNIGRIP, LATEX SURGICAL GLOVE, POWDER FREE | OMNI INTL., INC. |
| K984066 | 11/16/1998 | OMNIGRIP, LATEX SURGICAL GLOVE, POWDER-FREE WITH PROTEIN LABELING CLAIM | OMNI INTL., INC. |
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