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Oscillometric Blood Pressure Monitor

Page Type
Cleared 510(K)
510(k) Number
K190927
510(k) Type
Traditional
Applicant
Rudolf Riester GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/24/2019
Days to Decision
76 days
Submission Type
Summary

Oscillometric Blood Pressure Monitor

Page Type
Cleared 510(K)
510(k) Number
K190927
510(k) Type
Traditional
Applicant
Rudolf Riester GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/24/2019
Days to Decision
76 days
Submission Type
Summary