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FDA 510(k) Applications Submitted by ENDOTHELIX, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K072919
10/15/2007
VENDYS, MODEL 6000 B B/C
ENDOTHELIX, INC.
K060980
04/10/2006
VENDYS MODEL 5000 B/BC
ENDOTHELIX, INC.
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