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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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