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IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063057
510(k) Type
Abbreviated
Applicant
DIAGNOSTIC PRODUCTS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
78 days
Submission Type
Summary

IMMULITE/IMMULITE 1000, IMMULITE 2000 HIGH SENSITIVITY CRP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063057
510(k) Type
Abbreviated
Applicant
DIAGNOSTIC PRODUCTS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/2006
Days to Decision
78 days
Submission Type
Summary