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MODIFICATION TO PROFLU+ ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081030
510(k) Type
Special
Applicant
PRODESSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2008
Days to Decision
21 days
Submission Type
Summary

MODIFICATION TO PROFLU+ ASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081030
510(k) Type
Special
Applicant
PRODESSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2008
Days to Decision
21 days
Submission Type
Summary