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Yxoss CBR®

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192747
510(k) Type
Traditional
Applicant
Reoss GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/17/2020
Days to Decision
261 days
Submission Type
Summary

Yxoss CBR®

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192747
510(k) Type
Traditional
Applicant
Reoss GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
6/17/2020
Days to Decision
261 days
Submission Type
Summary