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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