FDA 510(k) Applications Submitted by LAURA LEBARRON

FDA 510(k) Number Submission Date Device Name Applicant
K964687 09/17/1996 N LATEX CRP MONO REAGENT BEHRING DIAGNOSTICS, INC.
K964062 10/10/1996 N PROTEIN STRANDARD SL BEHRING DIAGNOSTICS, INC.
K964065 10/10/1996 N/T PROTEIN CONTROL SL BEHRING DIAGNOSTICS, INC.


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