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Aptus Endosystems, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130677 APTUS HELI-FX AORTIC SECUREMENT SYSTEMOTD2013-04-12 View
510(k) K121168 APTUS 18FR HELIFX GUIDE-22 DEFLECTABLE LENGTHOTD2012-08-08 View
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