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FDA 510(k) Applications Submitted by DEAN A KNIGHT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K110687
03/11/2011
RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL)
ACCLARENT, INC.
K001258
04/18/2000
BX TRANSHEPATIC BILIARY STENT AND DELIVERY SYSTEM
CORDIS CORP.
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