# K000125: Jet Port Plus Catheter System

- Pathway: 510(k) (Traditional)
- Applicant: Clinical Plastic Products SA
- Decided: Apr 12, 2000 after 85 days
- Product code: LJT (Port & Catheter, Implanted, Subcutaneous, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5965
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
0 of 9 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
- 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
- K122767: Nmi Port (2013), 3 descendants of its own
- K131694: Nmi Port II Catheter (2013), 2 descendants of its own

## Recalls of this device
- Jan 28, 2015 · Class II · Z-1527-2015: The dual port with catheters was not covered under FDA clearance.

Source page: https://510kreport.com/device/K000125
Methodology: https://510kreport.com/methodology