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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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