FDA 510(k) Applications Submitted by MCPHERSON ENTERPRISES, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061484 | 05/30/2006 | MODIFICATION TO: SMITHWICK CAROTID SHUNT | MCPHERSON ENTERPRISES, INC. |
| K062474 | 08/24/2006 | SMITHWICK CAROTID SHUNT | MCPHERSON ENTERPRISES, INC. |
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