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Mcpherson Enterprises, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K061484 MODIFICATION TO: SMITHWICK CAROTID SHUNTDXC2006-12-07 View
510(k) K062474 SMITHWICK CAROTID SHUNTDXC2006-11-09 View
510(k) K823565 MULTI-LUMEN INTRAVENOUS CATHETERFOZ1982-12-16 View
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