# K930473: Onecath L-Cath Catheter System

- Pathway: 510(k) (Traditional)
- Applicant: Luther Medical Products, Inc.
- Decided: Apr 7, 1994 after 434 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 1 cites it directly.
0 of 7 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
- K980090: Onecath, L-Cath Catheter System, Model OC-(16-22 GA., 5CM-60CM) (1998), 5 descendants of its own
- K992424: Seldiflex Long-Term Central Venous Catheter (40CM & 60CM in Length), Models 63244J20 & 63246J20 (2000), 4 descendants of its own
- K063363: Firmgrip Peripherally Inserted Catheter Device (2007), 3 descendants of its own
- K080793: Firmgrip (2008), 2 descendants of its own
- K092629: SNM Firmgrip (2009), 1 descendant of its own

Source page: https://510kreport.com/device/K930473
Methodology: https://510kreport.com/methodology