FDA 510(k) Applications Submitted by KATHY SALFINGERE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K954967 | 10/30/1995 | GUTHRIE POWDERFREE LATEX EXAMINATION GLOVES | GUTHRIE MEDICARE PRODUCTS (MELAKA) SDN BHD |
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