# K130850: Primi and Secondi Support Catheters

- Pathway: 510(k) (Traditional)
- Applicant: Thermopeutix, Inc.
- Decided: Jun 25, 2013 after 90 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K132701: Primi Support Catheter (2013), 2 descendants of its own
- K183305: Crossing Support Catheter (2019), 0 descendants of its own
- K180889: Tractus Crossing Support Catheter (2018), 0 descendants of its own

Source page: https://510kreport.com/device/K130850
Methodology: https://510kreport.com/methodology