# K912702: Plastic Attachable Dual Port

- Pathway: 510(k) (Traditional)
- Applicant: Davol, Inc.
- Decided: Sep 18, 1991 after 91 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; 3 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K032044: X-Prot Duo Port (2003), 2 descendants of its own
- K133335: Powerport Implantable Port (2014), 0 descendants of its own
- K034065: Modification to X-Port Duo Port (2004), 0 descendants of its own
- K964066: Dual Slim Port Implanted Port (0654970/0654940) (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K912702
Methodology: https://510kreport.com/methodology