FDA 510(k) Applications Submitted by NxThera, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K150786 03/25/2015 Rezum System NxThera, Inc.
K160417 02/16/2016 Rezum System NxThera, Inc.
K180237 01/29/2018 Rezum System NxThera, Inc.


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