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PulsioFlex Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K172259
510(k) Type
Traditional
Applicant
PULSION Medical Systems SE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/18/2018
Days to Decision
175 days
Submission Type
Summary

PulsioFlex Monitoring System

Page Type
Cleared 510(K)
510(k) Number
K172259
510(k) Type
Traditional
Applicant
PULSION Medical Systems SE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
1/18/2018
Days to Decision
175 days
Submission Type
Summary