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


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact