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IMMULITE HIGH SENSITIVITY CRP, IMMULITE 2000 HIGH SENSITIVITY CRP

Page Type
Cleared 510(K)
510(k) Number
K003372
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/2000
Days to Decision
57 days
Submission Type
Summary

IMMULITE HIGH SENSITIVITY CRP, IMMULITE 2000 HIGH SENSITIVITY CRP

Page Type
Cleared 510(K)
510(k) Number
K003372
510(k) Type
Traditional
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/26/2000
Days to Decision
57 days
Submission Type
Summary