Rhythm Xience, Inc. (Rxi) is one of 18437 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rhythm Xience, Inc. (Rxi) - FDA 510(k) Cleared Devices
Recent clearances: Guider Catheter Introducer, Flextra Steerable Introducer
2
Total
2
Cleared
0
Denied
Rhythm Xience, Inc. (Rxi) has 2 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 2 cleared submissions from 2017 to 2017. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Rhythm Xience, Inc. (Rxi) Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Rhythm Xience, Inc. (Rxi)
2 devices