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PulsioFlex Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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