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MODIFICATION TO PROFLU+ ASSAY

Page Type
Cleared 510(K)
510(k) Number
K092500
510(k) Type
Special
Applicant
PRODESSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2009
Days to Decision
6 days
Submission Type
Summary

MODIFICATION TO PROFLU+ ASSAY

Page Type
Cleared 510(K)
510(k) Number
K092500
510(k) Type
Special
Applicant
PRODESSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/2009
Days to Decision
6 days
Submission Type
Summary