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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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