# K900677: Accent DG (TM) Balloon Angioplasty Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cook, Inc.
- Decided: Feb 22, 1991 after 375 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.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K012225: Attain 6215 Venogram Balloon Catheter (2001), 1 descendant of its own
- K121219: Attain Clarity 6225 Venogram Balloon Catheter (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K900677
Methodology: https://510kreport.com/methodology