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FDA 510(k) Applications Submitted by AM USA
FDA 510(k) Number
Submission Date
Device Name
Applicant
K111034
04/13/2011
AM USA 0.9% SODIUM CHLORIDE FLUSH SYRINGE
AM USA
K113555
12/01/2011
AM USA 0.9% SODIUM CHLORIDE FLUSH SYRINGE
AM USA
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