FDA 510(k) Applications Submitted by OMNI SALES CORP.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970297 | 01/27/1997 | OMNI GRIP LATEX EXAMINATION GLOVE, POWDER-FREE | OMNI SALES CORP. |
| K964563 | 11/14/1996 | OMNI GRIP LATEX EXAMINATION GLOVE, POWDER-FREE | OMNI SALES CORP. |
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