# K111850: Vaccess Pta Dilatation Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jul 13, 2011 after 14 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.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K120971: Atlas Pta Balloon Dilatation Catheter (2012), 9 descendants of its own
- K122984: Atlas Gold Pta Dilatation Catheter (2012), 7 descendants of its own
- K122367: Bard PTV Dilatation Catheter (2012), 5 descendants of its own
- K181323: Atlas Gold PTA Dilatation Catheter (2018), 4 descendants of its own
- K131002: Vida PTV Dilataton Catheter (2013), 4 descendants of its own

Source page: https://510kreport.com/device/K111850
Methodology: https://510kreport.com/methodology