# K926139: Cathlink 20 Titanium Port W/Att. Polyurethane Cath

- Pathway: 510(k) (Traditional)
- Applicant: Bard Access Systems, Inc.
- Decided: Jan 3, 1995 after 757 days
- Product code: LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5965
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K163001: PowerFlow Apheresis I.V. Port (2017), 2 descendants of its own
- K192291: TidalPort-AP Implantable Apheresis Vascular Access Port (2020), 0 descendants of its own
- K191143: PowerFlow Implantable Apheresis IV Port (2019), 0 descendants of its own
- K130873: Vwing Vascular Needle Guide, 4MM X 07MM; Vwing Vascular Needle Guide, 6MM X 07MM; Vwing Vascular Needle Guide, 8MM X 07M (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K926139
Methodology: https://510kreport.com/methodology