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VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE RANGE VERIFIERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011463
510(k) Type
Special
Applicant
Ortho-Clinical Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2001
Days to Decision
30 days
Submission Type
Summary

VITROS IMMUNODIAGNOSTIC PRODUCTS FOLATE RANGE VERIFIERS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011463
510(k) Type
Special
Applicant
Ortho-Clinical Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/13/2001
Days to Decision
30 days
Submission Type
Summary