# K864349: Mediport II Single Lum/Port Implant Vasc Acs Port

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Feb 10, 1987 after 98 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.
21 later devices descend from it; 1 cites it directly.
0 of 22 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
- K070003: Power Injectable Implantable Infusion Port with Silicone Lumen (Attachable and Pre-Attached) (2007), 20 descendants of its own
- K091099: C-Port - HP Power Injectable Port (2009), 5 descendants of its own
- K072481: Jet Port Plus HP Catheter System (2008), 5 descendants of its own
- K071993: T-Port HP Infusion Port (2007), 5 descendants of its own
- K073210: Modification to: T-Port HP Infusion Port (2007), 4 descendants of its own

Source page: https://510kreport.com/device/K864349
Methodology: https://510kreport.com/methodology