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IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K083853
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2009
Days to Decision
90 days
Submission Type
Summary

IMMULITE 2000 3GALLERGY SPECIFIC IGE ASSAY KIT

Page Type
Cleared 510(K)
510(k) Number
K083853
510(k) Type
Traditional
Applicant
SIEMENS HEALTHCARE DIAGNOSTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/24/2009
Days to Decision
90 days
Submission Type
Summary