# K131002: Vida PTV Dilataton Catheter

- Pathway: 510(k) (Traditional)
- Applicant: C.R. Bard, Inc.
- Decided: Jul 2, 2013 after 83 days
- Product code: OMZ (Pulmonary (Pulmonic) Valvuloplasty Catheters/Percutaneous Valvuloplasty Catheter)
- 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
Longest line of descent: 6 generations back to K933483 (1993). 12 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 17 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122367: Bard PTV Dilatation Catheter, C.R. Bard, Inc. (2012) Summary page 1.
- K122984: Atlas Gold Pta Dilatation Catheter, C.R. Bard, Inc. (2012) Summary page 1.

## Most influential descendants
- K141985: True BA V Balloon Valvuloplasty Catheter (2014), 3 descendants of its own
- K212588: Conquest 40 PTA Dilatation Catheter, Atlas Gold PTA Dilatation Catheter, Vida PTV Dilatation Catheter, Vida BAV Balloon Valvuloplasty Catheter (2022), 2 descendants of its own
- K241040: Amethyst HP PTA OTW 0.035 Catheter (2024), 1 descendant of its own
- K251915: Amethyst HP PTA OTW 0.035 Catheter (2025), 0 descendants of its own

## Indications for use
The Vida PTV Dilatation Catheter is recommended for Percutaneous Transluminal Valvuloplasty (PTV) of the pulmonary valve in the following: * A patient with isolated pulmonary valve stenosis * A patient with valvular pulmonary stenosis with other minor congenital heart disease that does not require surgical intervention.

Source page: https://510kreport.com/device/K131002
Methodology: https://510kreport.com/methodology