# K955839: Multi-Med Multi-Lumen Central Venous Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Edwards
- Decided: Mar 25, 1996 after 90 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: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
1 of 4 devices in its family (counting itself) has 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
- K091709: Multi-Med Central Venous Catheters, Models: M3720HKIC, M4820HKIC (2009), 2 descendants of its own
- K160747: Angel Catheter (2016), 0 descendants of its own
- K113565: Multi-Med Central Venous Catheters (CVCS), with and Without Heparin Vantex Central Venous Catheters (CVCS), with Heparin (2012), 0 descendants of its own

## Recalls of this device
- Oct 21, 2016 · Class I · Z-0647-2017: The kits contain Multi-Med Single Lumen Catheters that have a potential for excess material to remain at the tip of the catheter from the manufacturing process. It is possible that the excess material

Source page: https://510kreport.com/device/K955839
Methodology: https://510kreport.com/methodology