Last synced on 25 January 2026 at 3:41 am

K-ASSAY D-DIMER, K-ASSAY D-DIMER CALIBRATOR, MODELS KAI-090; KAJ-091C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030687
510(k) Type
Traditional
Applicant
Kamiya Biomedical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2003
Days to Decision
114 days
Submission Type
Statement

K-ASSAY D-DIMER, K-ASSAY D-DIMER CALIBRATOR, MODELS KAI-090; KAJ-091C

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K030687
510(k) Type
Traditional
Applicant
Kamiya Biomedical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/27/2003
Days to Decision
114 days
Submission Type
Statement