FDA 510(k) Applications Submitted by SUSAN OLINGER

FDA 510(k) Number Submission Date Device Name Applicant
K130943 04/04/2013 AIGIS RX R PM/ AIGIS RX R ICD TYRX , INC.
K131007 04/11/2013 AIGIS RX N MEDIUM; AIGIS RX N LARGE TYRX ,INC
K071518 06/04/2007 DIACAP LO PS (10, 12, 15) AND DIACAP HI PS (10, 12, 15, 18, 20) HEMODIALYZERS B. BRAUN MEDIZINTECHNOLOGIE GMBH
K092313 07/30/2009 PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEM B. BRAUN MEDICAL, INC.


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