# K992424: Seldiflex Long-Term Central Venous Catheter (40CM & 60CM in Length), Models 63244J20 & 63246J20

- Pathway: 510(k) (Traditional)
- Applicant: Plastimed Laboratoire Pharmaceutique
- Decided: Dec 29, 2000 after 527 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
Longest line of descent: 2 generations back to K930473 (1994). 3 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K823553: Corcath H & B Vascular Access Catheter, Cormed, Inc., Sub. C.R.Bard, Inc. (1983) Summary page 1.
- K980090: Onecath, L-Cath Catheter System, Model OC-(16-22 GA., 5CM-60CM), Luther Medical Products, Inc. (1998) Summary page 1.

## Most influential descendants
- 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
- K111939: M/29TM - Pressure Injectable (2012), 0 descendants of its own

## Indications for use
Plastimed’s Seldiflex® central venous catheter is intended for long-term vascular access and is indicated for use with patients who require central venous pressure monitoring, L.V. fluids, blood products, drugs, or parenteral nutrition solutions.

Source page: https://510kreport.com/device/K992424
Methodology: https://510kreport.com/methodology