FDA 510(k) Applications Submitted by Rex Medical, L.P.

FDA 510(k) Number Submission Date Device Name Applicant
K191419 05/28/2019 Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire Rex Medical, L.P.
K212351 07/29/2021 Revolution Peripheral Atherectomy System Rex Medical, L.P.
K173389 10/30/2017 Rex Medical Aspiration Pump Rex Medical, L.P.
K141617 06/17/2014 CLEANER ROTATIONAL THROMBECTOMY SYSTEM REX MEDICAL, L.P.


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