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SEKURE Creatine Kinase Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182702
510(k) Type
Traditional
Applicant
Sekisui Diagnostics P.E.I., Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
202 days
Submission Type
Summary

SEKURE Creatine Kinase Assay

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182702
510(k) Type
Traditional
Applicant
Sekisui Diagnostics P.E.I., Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/17/2019
Days to Decision
202 days
Submission Type
Summary