FDA 510(k) Applications Submitted by ED LEE

FDA 510(k) Number Submission Date Device Name Applicant
K022071 06/26/2002 EMBOL-X AORTIC FILTERS,ETRA-SMALL,SMALL,MEDIUM,LARGE,EXTRA LARGE,MODELS CF26000.CF29000,CF32000,CF35000,CF4000 EMBOL-X, INC.
K002973 09/22/2000 EMBOL-X INTRODUCER, MODEL CF00200 EMBOL-X, INC.
K020693 03/04/2002 AORTIC CANNULA, METAL J-TIP (24FR) MODEL #CF00100; AORTIC CANNULA, PLASTIC J-TIP (24FR) MODEL #CF00101 EMBOL-X, INC.


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