# K861479: Cavafix, Central Venous Catheter Kit

- Pathway: 510(k) (Traditional)
- Applicant: Burron Medical Products, Inc.
- Decided: Jul 1, 1986 after 70 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- 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; 2 cite 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K971999: Peripherally Inserted Central (1997), 4 descendants of its own
- K031689: Dual Lumen Extended Length Catheter (Delc) (2003), 3 descendants of its own
- K041791: 5.2F Dual Lumen Extended Length Catheter (Delc) (2004), 2 descendants of its own
- K233515: Dual Lumen Extended Length Catheter (dELC), 6F, 12 cm (320101), Dual Lumen Extended Length Catheter (dELC), 6F, 16 cm (320102) (2023), 1 descendant of its own
- K252226: Dual Lumen Extended Length Catheter (dELC), 6F, 12cm (320101); Dual Lumen Extended Length Catheter (dELC), 6F, 16 cm (320102) (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K861479
Methodology: https://510kreport.com/methodology