FDA 510(k) Applications Submitted by JK GLOVES SDN. BHD.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K010231 | 01/24/2001 | JK GLOVES PRE-POWDERED LATEX EXAMINATION GLOVE | JK GLOVES SDN. BHD. |
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