3T Vessel Cannulas
510(k) K020768
3T Vessel Cannulas is a medical device (FDA Class II; FDA product code DWF, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass) made by 3t Medical Systems, LLC, cleared under FDA 510(k) K020768 on 23 Aug 2002, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK020768 | Date23 Aug 2002 | StatusActive |
Official records
- FDA 510(k) database K020768
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- DWF
- Device class
- Class II
- Regulation
- 21 CFR Part 870.4210
- Advisory committee
- Cardiovascular
- FDA decision
- SESE Substantially Equivalent
Similar devices
Other devices filed under FDA product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass).
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- TENDERFLOW PERIATRIC ARTERIAL CANNULA by Terumo Cardiovascular Systems Corporation
- Vessel Cannula, 3mm VCC-03 by QUEST MEDICAL INC
- Churchill Inter-Cardiac Sucker by Churchill Corp.
- TandemHeart Veno-Venous Cannula by CARDIACASSIST, INC.
- Signature Custom Tubing Pack by Avecor Cardiovascular, Inc.
- Better-Tubing by Circulatory Technology, Inc.
- Modified Coronary Cardioplegia Adaptor by Shiley, Inc.