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K-ASSAY MYOGLOBIN ASSAY, K-ASSAY MYOGLOBIN CALIBRATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992976
510(k) Type
Traditional
Applicant
Kamiya Biomedical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1999
Days to Decision
59 days
Submission Type
Statement

K-ASSAY MYOGLOBIN ASSAY, K-ASSAY MYOGLOBIN CALIBRATOR

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992976
510(k) Type
Traditional
Applicant
Kamiya Biomedical Co.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1999
Days to Decision
59 days
Submission Type
Statement