FDA 510(k) Applications Submitted by SIENNA BIOTECH, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K955799 12/22/1995 COPALIS CMV TOTAL ANTIBODY ASSAY SIENNA BIOTECH, INC.
K970931 03/07/1997 COPALIS TORC TOTAL ANTIBODY ASSAY SIENNA BIOTECH, INC.
K961784 05/02/1996 COPALIS ONE IMMUNOASSAY SYSTEM/TOXOPLASMA GONDII/RUBELLA/CMV TOTAL ANTIBODY ASSAYS SIENNA BIOTECH, INC.


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