# K000855: Gunther Tulip Vena Cava Mreye Filter Set

- Pathway: 510(k) (Traditional)
- Applicant: Cook, Inc.
- Decided: Oct 18, 2000 after 216 days
- Product code: DTK (Filter, Intravascular, Cardiovascular)
- Device class: 2
- Regulation: 21 CFR 870.3375
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
33 later devices descend from it; 3 cite it directly.
3 of 34 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
- K032426: Gunhter Tulip Vena Cava Mreye Filter and Retrieval Set (2003), 31 descendants of its own
- K061815: Cook Celect Vena Cava Filter (2007), 17 descendants of its own
- K073374: Cook Clect Vena Cava Filter, Gunther Tulip Vena Cava Filter Retrieval Set (2008), 16 descendants of its own
- K112185: Foursnare Vascular Retrieval Snare (2011), 6 descendants of its own
- K081410: Option Vena Cava Filter (2009), 6 descendants of its own

Source page: https://510kreport.com/device/K000855
Methodology: https://510kreport.com/methodology