FDA 510(k) Applications Submitted by KATHLEEN VITTUM
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K080154 | 01/23/2008 | ACUITY UNIVERSAL CUTTER | CARDIAC PACEMAKERS, INC. |
| K061453 | 05/25/2006 | HI-TORQUE WHISPER VIEW GUIDE WIRE | GUIDANT CORP. |
| K093969 | 12/23/2009 | ACUITY BREAK-AWAY GUIDE CATHETER | CARDIAC PACEMAKERS, INC. |
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