FDA 510(k) Applications Submitted by Suzanne Grenier

FDA 510(k) Number Submission Date Device Name Applicant
K130333 02/11/2013 CAPIX RX HOLLOW FIBER OXYGENATOR WITH/WITHOUT HARDSHELL RESERVOIR TERUMO CARDIOVASCULAR SYSTEMS CORP.
K130359 02/13/2013 CAPIOX SX18 HOLLOW FIBER OXYGENATOR WITH DETACHABLE HARDSHELL RESERVOIR, CAPIOX SX25 HOLLOW FIBER OXGENATOR WITH DETACHA TERUMO CARDIOVASCULAR SYSTEMS CORP.
K121209 04/20/2012 TERUMO PALL AL20X ARTERIAL FILTER Terumo Cardiovascular Systems Corporation
K142500 09/05/2014 One Way Soft Valve Terumo Cardiovascular Systems Corporation


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