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FDA 510(k) Applications Submitted by DEBORA STAPLETON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K112511
08/30/2011
DOBBHOFF DUAL PORT FEEDING TUBE
COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
K073122
11/06/2007
MONOJECT HYPODERMIC NEEDLE, MODEL 250, 30 GAUGE HYPODERMIC NEEDLE
COVIDIEN LP, FORMERLY REGISTERED AS TYCO HEALTHCAR
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