Last synced on 25 January 2026 at 3:41 am

IMMULITE 2000 ALLERGEN-SPECIFIC IGE

Page Type
Cleared 510(K)
PDF
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
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