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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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