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FDA 510(k) Applications Submitted by DAVID LERNER
FDA 510(k) Number
Submission Date
Device Name
Applicant
K973644
09/24/1997
FLOSTAT VASCULAR LAB
BIOMEDIX, INC.
K973857
10/09/1997
FLOSTAT VASCULAR REPORT GENERATOR (VRG)
BIOMEDIX, INC.
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