510(k) · Cleared
Recalled · Class II · 2015Jet Port Plus Catheter System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Clinical Plastic Products SA · LJT Port & Catheter, Implanted, Subcutaneous, Intravascular
Cleared on Apr 12, 2000 after an 85-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 8 later devices descend from it. It has been recalled once.
- Decided
- Apr 12, 2000
- Review
- 85 days
- Class
- Class II
- Product code
- LJT
- Recalls
- 1
- Predicates
- 0
8 later devices descend from it, 2 citing it directly.
- This deviceK000125 Jet Port Plus Catheter SystemClinical Plastic Products SA · 2000
- Descendant · cites it directly · 5 of its ownK072481 Jet Port Plus HP Catheter SystemPfm Medical, Inc. · 2008
- Descendant · cites it directly · 5 of its ownK071993 T-Port HP Infusion PortPfm Medical, Inc. · 2007
- Descendant · 2 generations on · 4 of its ownK073210 Modification to: T-Port HP Infusion PortPfm Medical, Inc. · 2007
- Descendant · 2 generations on · 3 of its ownK122767 Nmi PortNavilyst Medical, Inc. · 2013 · Recalled
- Descendant · 3 generations on · 2 of its ownK131694 Nmi Port II CatheterNavilyst Medical, Inc. · 2013 · Recalled
Showing 5 of 8 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 8 · See all- K072481Jet Port Plus HP Catheter SystemPfm Medical, Inc. · 2008 · cites it directly5descendants
- K071993T-Port HP Infusion PortPfm Medical, Inc. · 2007 · cites it directly5descendants
- K073210Modification to: T-Port HP Infusion PortPfm Medical, Inc. · 2007 · 2 generations on4descendants
- K122767Nmi PortNavilyst Medical, Inc. · 2013 · 2 generations on3descendants
- K131694Nmi Port II CatheterNavilyst Medical, Inc. · 2013 · 3 generations on2descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K000125 | Jet Port Plus Catheter System | Clinical Plastic Products SA | 2000 | — |
| +1 | K072481 | Jet Port Plus HP Catheter System | Pfm Medical, Inc. | 2008 | — |
| +1 | K071993 | T-Port HP Infusion Port | Pfm Medical, Inc. | 2007 | — |
| +2 | K073210 | Modification to: T-Port HP Infusion Port | Pfm Medical, Inc. | 2007 | — |
| +2 | K122767 | Nmi Port | Navilyst Medical, Inc. | 2013 | 6 |
| +3 | K131694 | Nmi Port II Catheter | Navilyst Medical, Inc. | 2013 | 2 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 2 | 0 |
| 2008 | 1 | 0 |
| 2013 | 3 | 0 |
| 2015 | 1 | 0 |
| 2020 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in LJT? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new LJT device
- #1 K251253 PowerPort™ isp Implantable Port; PowerPort™…score 14.9 · 9 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (8)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 28, 2015 | Class II | Z-1527-2015 | PMA | The dual port with catheters was not covered under FDA clearance. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K072481 (Pfm Medical, Inc., 2008) has gone furthest, with 5 descendants of its own.
How does its category compare?
All LJT devicesLJT Port & Catheter, Implanted, Subcutaneous, Intravascular: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LJT
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LJT
182in 2016
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LJT
1in 2022
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · LJT
4,308in 2025
MAUDE reports naming product code LJT, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 11 | 85 | 1 | 208 |
| 2008 | 7 | 119 | 2 | 161 |
| 2009 | 2 | — | 2 | 172 |
| 2010 | 2 | — | 19 | 207 |
| 2011 | 5 | 144 | 1 | 202 |
| 2012 | 2 | — | 2 | 153 |
| 2013 | 7 | 150 | 0 | 141 |
| 2014 | 2 | — | 0 | 143 |
| 2015 | 4 | 164 | 1 | 149 |
| 2016 | 3 | 182 | 0 | 135 |
| 2017 | 0 | — | 1 | 262 |
| 2018 | 0 | — | 1 | 878 |
| 2019 | 1 | — | 7 | 765 |
| 2020 | 1 | — | 0 | 959 |
| 2021 | 0 | — | 0 | 1,285 |
| 2022 | 0 | — | 1 | 1,334 |
| 2023 | 1 | — | 0 | 1,221 |
| 2024 | 1 | — | 0 | 1,896 |
| 2025 | 2 | — | 0 | 4,308 |
| 2026 | 1 | — | 1 (1) | — |
https://510kreport.com/device/K000125 · printed Nov 5, 2026
Cite this page
510(k) Report. “K000125: Jet Port Plus Catheter System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K000125
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026