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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