FDA 510(k) Applications Submitted by MICHELLE STRAIGHT
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K140557 | 03/05/2014 | MIVI 6F GUIDE CATHETER | MIVI, LLC |
| K111987 | 07/13/2011 | FIBERNET EMBOLIC PROTECTION DEVICE | LUMEN BIOMEDICAL, INC. |
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