# K032044: X-Prot Duo Port

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Jul 10, 2003 after 8 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
Longest line of descent: 1 generation back to K912702 (1991). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K912702: Plastic Attachable Dual Port, Davol, Inc. (1991) Summary page 1.

## Most influential descendants
- K133335: Powerport Implantable Port (2014), 0 descendants of its own
- K034065: Modification to X-Port Duo Port (2004), 0 descendants of its own

## Indications for use
The BardPort®, SlimPort™ and X-Port™ Implanted Ports are indicated for patient therapies requiring repeated access to the vascular system. The port system can be used for infusion of medications, I.V. fluids, parenteral nutrition solutions, blood products and for the withdrawal of blood samples.

Source page: https://510kreport.com/device/K032044
Methodology: https://510kreport.com/methodology