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CardioPhase® hsCRP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212559
510(k) Type
Special
Applicant
Siemens Healthcare Diagnostics Products GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
490 days
Submission Type
Summary

CardioPhase® hsCRP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212559
510(k) Type
Special
Applicant
Siemens Healthcare Diagnostics Products GmbH
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
12/16/2022
Days to Decision
490 days
Submission Type
Summary