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PulsioFlex Monitoring System with ProAQT Sensor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192169
510(k) Type
Traditional
Applicant
Pulsion Medical Systems SE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
265 days
Submission Type
Summary

PulsioFlex Monitoring System with ProAQT Sensor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192169
510(k) Type
Traditional
Applicant
Pulsion Medical Systems SE
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
265 days
Submission Type
Summary