# K010831: Aviator Peripheral Dilatation Catheter

- Pathway: 510(k) (Special)
- Applicant: Guidant Corp.
- Decided: Jun 13, 2001 after 85 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.
66 later devices descend from it; 1 cites it directly.
0 of 67 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
- K013581: Cordis Aviator Peripheral Dilatation Catheter (2001), 65 descendants of its own
- K050629: Angiosculpt Scoring Balloon Catheter (2005), 38 descendants of its own
- K072225: Angiosculpt Pta Scoring Balloon Catheter (2007), 37 descendants of its own
- K080151: Angiosculpt Pta Scoring Balloon Catheter, Models 2076 and 2039 (2008), 36 descendants of its own
- K082059: Angiosculpt Pta Scoring Balloon Catheter (2008), 34 descendants of its own

Source page: https://510kreport.com/device/K010831
Methodology: https://510kreport.com/methodology