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IMMULITE 2000 ALLERGEN-SPECIFIC IGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023152
510(k) Type
Abbreviated
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2002
Days to Decision
85 days
Submission Type
Summary

IMMULITE 2000 ALLERGEN-SPECIFIC IGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023152
510(k) Type
Abbreviated
Applicant
DIAGNOSTIC PRODUCTS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/17/2002
Days to Decision
85 days
Submission Type
Summary