FDA 510(k) Applications Submitted by WILLIAM MCPHERSON

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.
K021608 05/16/2002 SMITHWICK CAROTID SHUNT IMPLANTABLE DEVICES
K963813 09/23/1996 SURE CORE BIOPSY KIT INTERVENTIONAL CONCEPTS, INC.


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