FDA 510(k) Applications Submitted by EDWARD (TED) WULFMAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K141218 | 05/12/2014 | ZIGIWIRE MODE2 GUIDEWIRE WIRE SYSTEM, ZIGIWIRE MODE3 GUIDEWIRE WIRE SYSTEM | VADISWIRE CORPORATION |
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