FDA 510(k) Applications Submitted by AMY ESKINA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110055 | 01/10/2011 | REVERSE MEDICAL REFLEX GUIDE CATHETER | REVERSE MEDICAL CORPORATION |
| K091563 | 05/28/2009 | RECRUIT MICROCATHETER | REVERSE MEDICAL CORPORATION |
| K102418 | 08/25/2010 | REVERSE MEDICAL REPORT GUIDE CATHETER SYSTEM | REVERSE MEDICAL CORPORATION |
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