FDA 510(k) Applications Submitted by Enterix Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K060930 04/05/2006 INSURE II ENTERIX INC.
K170548 02/24/2017 InSure ONE Enterix Inc.
K002457 08/10/2000 !NSURE FECAL OCCULT BLOOD TEST ENTERIX INC.


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