Trio-CT Triple Lumen Catheter

No FDA recalls on record, checked 9 Oct 2026.

510(k) Number

K183219 ↗

FDA Product Code

NIE

Device Class

Class II

Regulation

21 CFR Part 876.5540

Advisory Committee

Gastroenterology, Urology

FDA Decision

SEKD

• C3 Wave System

  Class II

  FDA 510(k) K170934 Active Cleared 6 Dec 2017

• Trio-CT­® Triple Lumen Catheter w/ Curved Extensions

  Class II

  FDA 510(k) K232945 Active Cleared 16 Nov 2023

• 15.5F X 19 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 23 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 28 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 33 cm Symetrex Long Term Hemodialysis Catheter with Sideholes, 15.5F X 37 cm Symetrex Long Term Hemodialysis Catheter with Sideholes

  Class II

  FDA 510(k) K173667 Active Cleared 17 May 2018

• CT Midline

  Class II

  FDA 510(k) K170770 Active Cleared 25 Jul 2017

• Symetrex LTHD Catheter, Symetrex LTHD Catheter with Sideholes

  Class II

  FDA 510(k) K202176 Active Cleared 3 Sep 2020

• Duo-Flow Side x Side Double Lumen Catheter

  Class II

  FDA 510(k) K192807 Active Cleared 23 Apr 2020

See all devices from Medical Components, Inc. (dba MedComp) →