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FDA 510(k) Applications Submitted by Pulsion Medical Systems SE
FDA 510(k) Number
Submission Date
Device Name
Applicant
K171620
06/02/2017
PiCCO Catheter
PULSION Medical Systems SE
K122121
07/17/2012
PULSIOFLEX MONITORING SYSTEM WITH PICCO MODULE
PULSION MEDICAL SYSTEMS SE
K172259
07/27/2017
PulsioFlex Monitoring System
PULSION Medical Systems SE
K192169
08/09/2019
PulsioFlex Monitoring System with ProAQT Sensor
Pulsion Medical Systems SE
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