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FDA 510(k) Applications Submitted by MICHELLE B ROEDING
FDA 510(k) Number
Submission Date
Device Name
Applicant
K140733
03/24/2014
CONSTELLATION MULTIPLE ELECTRODE RECORDING & PACING CATHETER
Boston Scientific Corporation
K051215
05/12/2005
CELL-DYN SAPPHIRE SYSTEM
ABBOTT LABORATORIES
K061667
06/14/2006
CELL-DYN RUBY SYSTEM
ABBOTT LABORATORIES
K110381
02/10/2011
CELL-DYN EMERALD 22 SYSTEM
ABBOTT LABORATORIES
K991605
05/10/1999
CELL-DYN 3500 SYSTEM WITH IMMATURE RETICULOCYTE FRACTION (IRF), CELL-DYN 3700 SYSTEM WITH IMMATURE RETICULOCYTE FRACTION
ABBOTT LABORATORIES
K081495
05/29/2008
CELL-DYN EMERALD SYSTEM
ABBOTT LABORATORIES
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