FDA 510(k) Applications Submitted by MYELOTEC, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K960194 | 01/16/1996 | MYELOTEC MYELOSCOPE | MYELOTEC, INC. |
| K980734 | 02/25/1998 | MYELOTEC VIDEO GUIDED CATHETER | MYELOTEC, INC. |
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