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FDA 510(k) Applications Submitted by Rhythm Xience, Inc. (RXI)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170373
02/07/2017
Flextra Steerable Introducer
Rhythm Xience, Inc. (RXI)
K171081
04/11/2017
Guider Catheter Introducer
Rhythm Xience, Inc. (RXI)
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