FDA 510(k) Applications Submitted by DAVID A GREER
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110936 | 04/04/2011 | DURAFLOW 2 CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT | ANGIODYNAMICS, INC. |
| K101843 | 07/01/2010 | DURAMAX CHRONIC HEMODIALYSIS CATHETER AND PROCEDURE KIT | ANGIODYNAMICS, INC. |
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