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IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093107
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
364 days
Submission Type
Summary

IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093107
510(k) Type
Traditional
Applicant
Siemens Healthcare Diagnostics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2010
Days to Decision
364 days
Submission Type
Summary