FDA 510(k) Applications Submitted by MEDI-DYNE, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K970401 | 02/03/1997 | MEDI-DYNE GUIDING CATHETER | MEDI-DYNE, INC. |
| K000825 | 03/14/2000 | 4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER | MEDI-DYNE, INC. |
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