# K862006: Stand & High Flow Femoral-Ventricular Pigtail Cath

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Jun 27, 1986 after 31 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K051561: Asahi Angiographic Catheter (2005), 2 descendants of its own
- K082559: Spectranetics Cross-Pilot Turbo Elite Support Catheter (2008), 1 descendant of its own
- K090913: Cross-Pilot Turbo Elite Support Catheter (2009), 0 descendants of its own
- K970469: Evt Angioscale Angiographic Catheter (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K862006
Methodology: https://510kreport.com/methodology