FDA 510(k) Applications Submitted by JOHN CALHOUN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K081910 | 07/03/2008 | NON-STERILE, POWDERED LATEX EXAMINATION GLOVE | SIAM SEMPERMED CORP. LTD. |
| K021220 | 03/22/2002 | NITRILE PATIENT EXAMINATION GLOVE POWDER-FREE (BLUE COLOR) TESTED FOR USE WITH CHEMOTHERAPY DRUGS | SIAM SEMPERMED CORP. LTD. |
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