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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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