FDA 510(k) Applications Submitted by POONSUK CHERDKIATGUMCHAI
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970794 | 03/04/1997 | LATEX PATIENT EXAMINATION (POWDERFREE GLOVE) | SIAM SEMPERMED CORP. LTD. |
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