QHW
- 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.
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K251831 | 2026-01-15 | Medtronic, Inc. | Bio-Medicus Life Support Catheter and Introducer | |
| K240534 | 2024-04-19 | Medtronic, Inc. | Bio-Medicus Life Support Catheter and Introducer |
Official FDA classification page: QHW
Classification and pathway per current FDA publications. Data from openFDA (CC0).