FDA 510(k) Applications Submitted by DEBORAH BAKER-JANIS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093681 | 11/27/2009 | MERIDIAN GUIDEWIRE | EV3 NEUROVASCULAR |
| K112409 | 08/22/2011 | MATRISTEM WOUND MATRIX | ACELL, INC |
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