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IMMULITE/IMMULITE® 1000 Cortisol

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203270
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics Products, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/15/2021
Days to Decision
71 days
Submission Type
Summary

IMMULITE/IMMULITE® 1000 Cortisol

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203270
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics Products, Ltd.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
1/15/2021
Days to Decision
71 days
Submission Type
Summary