FDA 510(k) Applications Submitted by MARY DE ARMOND

FDA 510(k) Number Submission Date Device Name Applicant
K961917 05/17/1996 MEDTRONIC MUSTANG STEERABLE GUIDE WIRE (M-45FR, M45FX) MEDTRONICS INTERVENTIONAL VASCULAR
K896020 10/16/1989 EXTRACORPOREAL HEAT EXCHANGER "HE SERIES" GISH BIOMEDICAL, INC.
K896807 12/04/1989 SPBC SERIES SINGLE PASS BLOOD CARDIOPLEGIA SYSTEM GISH BIOMEDICAL, INC.
K991633 05/12/1999 QUICKVUE INFLUENZA A/B TEST QUIDEL CORP.
K972944 08/11/1997 MEDTRONIC MUSTANG SUPER FLOPPY GUIDE WIRE/FLOPPY GUIDE WIRE/INTERMEDIATE GUIDE WIRE/STANDARD GUIDE WIRE/EXTRA SUPPORT MEDTRONICS INTERVENTIONAL VASCULAR


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