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Medtronic Versaflex, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K891611 MODELS 6526,6527,6528 PERCU. TRANS. ANGIO. CATH.LJT1989-06-12 View
510(k) K890898 MODEL 611101 CONTRAST INJECTION DEVICEDXT1989-04-12 View
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