# K810412: Usci Cardiovascular Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Mar 5, 1981 after 15 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.
8 later devices descend from it; 1 cites it directly.
2 of 9 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
- K041909: Vascular Solutions Langston Dual Lumen Pigtail Catheter (DLP) (2004), 7 descendants of its own
- K061565: Langston Dual Lumen Catheter (2006), 6 descendants of its own
- K062627: Innerchange Micro-Introducer Catheter, Models 7900 Through 7905 (2007), 2 descendants of its own
- K170544: Langston dual lumen catheter (2017), 1 descendant of its own
- K073585: Innerchange Micro-Introducer Catheter, Models 7900, 7901, 7902, 7903, 7904 and 7905 (2008), 1 descendant of its own

Source page: https://510kreport.com/device/K810412
Methodology: https://510kreport.com/methodology