FDA 510(k) Applications Submitted by JEFF STURM
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070166 | 01/18/2007 | STRADA CAROTID GUIDING SHEATH | ST. JUDE MEDICAL |
| K082304 | 08/13/2008 | ROLL-X GUIDEWIRE | ST. JUDE MEDICAL |
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