FDA 510(k) Applications Submitted by MICHAEL FRIEDMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030849 | 03/17/2003 | AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1 | N-DIA, INC. |
| K081767 | 06/20/2008 | AMNISURE FETAL MEMBRANES RUPTURE TEST, MODEL FMRT-1 | AMNISURE INTERNATIONAL, LLC |
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