FDA 510(k) Applications Submitted by MICHELE WALZ
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K091825 | 06/19/2009 | HI-TORQUE PROGRESS GUIDE WIRE FAMILY | ABBOTT VASCULAR INC. |
| K072460 | 08/31/2007 | HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II GUIDE WIRE | ABBOTT VASCULAR, INC. |
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