FDA 510(k) Applications Submitted by MARTHA RUMFORD

FDA 510(k) Number Submission Date Device Name Applicant
K950739 02/17/1995 3M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEM 3M HEALTH CARE, SARNS
K171610 06/01/2017 MC3 QuickFlow Dual Lumen Catheter MC3 Incorporated
K113421 11/18/2011 MINICAT XORAN TECHNOLOGIES, INC.
K090191 01/27/2009 HANDYLAB GBS ASSAY, HANDYLAB JAGUAR INSTRUMENT, HANDYLAB DNA EXTRACTION STRIP, HANDYLAB E3 EXTRACTION REAGENT, HANDYLAB HANDYLAB, INC


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