FDA 510(k) Applications Submitted by RICK SPRING
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K090111 | 01/16/2009 | FLEXPEN NEEDLE | NOVO NORDISK INC. |
| K062500 | 08/25/2006 | FLEXPEN NEEDLE | NOVO NORDISK INC. |
| K133738 | 12/09/2013 | NOVOFINE PLUS 32G 4 MM | NOVO NORDISK INC. |
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