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VITROS IMMUNODIAGNOSTIC PRODUCTS CK-MB REAGENT PACK ; VITROS IMMUNODIAGNOSTIC PRODUCTS CK-MB CALIBRATORS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993068
510(k) Type
Special
Applicant
Ortho-Clinical Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1999
Days to Decision
21 days
Submission Type
Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS CK-MB REAGENT PACK ; VITROS IMMUNODIAGNOSTIC PRODUCTS CK-MB CALIBRATORS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K993068
510(k) Type
Special
Applicant
Ortho-Clinical Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/1999
Days to Decision
21 days
Submission Type
Summary