# K000101: RX Viatrac 14 Peripheral Dilatation Catheter

- Pathway: 510(k) (Special)
- Applicant: Guidant Corp.
- Decided: Feb 10, 2000 after 28 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- 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.
79 later devices descend from it; 4 cite it directly.
0 of 80 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
- K063657: Vascutrak Pta Dilation Catheter (2006), 52 descendants of its own
- K073025: Vascutrak II Pta Dilatation Catheter (2007), 48 descendants of its own
- K082343: Vascutrak 2, Models: V14 and V18 (2008), 47 descendants of its own
- K103459: Vascutrak Pta Dilatation Catheter (2010), 36 descendants of its own
- K100303: Angiosculpt Pta Scoring Balloon Catheter Model 2039-Xxyy, 2076-Xxyy, 2092-Xxyy, 2105-Xxyy (2010), 32 descendants of its own

Source page: https://510kreport.com/device/K000101
Methodology: https://510kreport.com/methodology