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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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