FDA 510(k) Applications Submitted by M/S MIDLAND LATEX PRODUCTS LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K982114 | 06/16/1998 | LOPRO SILICONISED LOW PROTEIN POWDERFREE LATEX EXAMINATION GLOVES | M/S MIDLAND LATEX PRODUCTS LTD. |
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