# K870067: Multicath - Code#S 8.1207.OO/8.1208.00/8.1205.20

- Pathway: 510(k) (Traditional)
- Applicant: Vygon Corp.
- Decided: Apr 28, 1987 after 110 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K061250: Multicath Expert (2006), 1 descendant of its own
- K072702: Stryker Antimic Catheter (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K870067
Methodology: https://510kreport.com/methodology