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AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES

Page Type
Cleared 510(K)
510(k) Number
K122197
510(k) Type
Traditional
Applicant
PHADIA US INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
400 days
Submission Type
Summary

AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES

Page Type
Cleared 510(K)
510(k) Number
K122197
510(k) Type
Traditional
Applicant
PHADIA US INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/28/2013
Days to Decision
400 days
Submission Type
Summary