QHW

Single Lumen Ecmo Cannula

Product code
QHW
Device name
Single Lumen Ecmo Cannula
Device class
Class 2
21 CFR
21 CFR 870.4100
Medical specialty
Cardiovascular
Marketing pathway
510(K)
510(k) clearances (last 3 years)
2
Summaries archived here
2 (direct download)
510(k) clearances (all years, FDA)
3 (all years; only the last 3 years are listed here)

FDA classification definition

Single-lumen cannulas/catheters to be used with an extracorporeal circuit intended for use in patients with acute respiratory failure or acute cardiopulmonary failure, where other available treatment options have failed, and continued clinical deterioration is expected or the risk of death is imminent.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (2)

Last three years. Most recent: 2026-01-15.

NumberDecision dateApplicantDevice nameSummary
K2518312026-01-15Medtronic, Inc.Bio-Medicus Life Support Catheter and IntroducerPDF
K2405342024-04-19Medtronic, Inc.Bio-Medicus Life Support Catheter and IntroducerPDF

2 summaries are archived here for direct download.

Official FDA classification page: QHW
Classification and pathway per current FDA publications. Data from openFDA (CC0).