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Sontek Corp.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K832279 PERIPHERAL TRANSLUMINAL ARGIOPLASTY1983-11-14 View
510(k) K831562 SONTEK INFUSION CATHETERDQO1983-06-30 View
510(k) K810508 SONTEK ANGIOGRAPHIC CATHETERDQO1981-04-17 View
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