FDA 510(k) Applications Submitted by H.B.M. USA CO.,INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K050071 | 01/12/2005 | MEDISPO (POWDERED) AND MEDISPO-PF (POWDER-FREE) SURGEONS GLOVE | H.B.M. USA CO.,INC. |
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