FDA 510(k) Applications Submitted by HANWELLA RUBBER PRODUCTS LTD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000351 | 02/04/2000 | HANWELLA LATEX PATIENT EXAM. GLOVES POWDER-FREE | HANWELLA RUBBER PRODUCTS LTD. |
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