# K864038: Supercath I.V. Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Togo Medikit Co., Ltd.
- Decided: Dec 4, 1986 after 49 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.
31 later devices descend from it; 1 cites it directly.
0 of 32 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
- K050114: Supercath Z3V (2005), 30 descendants of its own
- K081953: Supercath 5 (2009), 28 descendants of its own
- K093546: Supercath 5 Model SP120-XX-XX, SP125-XX-XX (2009), 27 descendants of its own
- K110443: BD Insyte Autoguard BC (2011), 21 descendants of its own
- K140504: Accucath BC Intravascular Catheter System (2014), 7 descendants of its own

Source page: https://510kreport.com/device/K864038
Methodology: https://510kreport.com/methodology