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IMMULITE 2000 ACTH CALIBRATION VERIFICATION MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K131662
510(k) Type
Abbreviated
Applicant
Siemens Healthcare Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2013
Days to Decision
125 days
Submission Type
Summary

IMMULITE 2000 ACTH CALIBRATION VERIFICATION MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K131662
510(k) Type
Abbreviated
Applicant
Siemens Healthcare Diagnostics Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2013
Days to Decision
125 days
Submission Type
Summary