# K915414: Terumo Angiogtaphic Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Terumo Medical Corp.
- Decided: Feb 4, 1992 after 64 days
- Product code: DQO (Catheter, Intravascular, Diagnostic)
- Device class: 2
- Regulation: 21 CFR 870.1200
- 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; 5 cite 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992051: Radifocus Optitorque (1999), 32 descendants of its own
- K082561: Spectranetics Quick-Cross Extreme Support Catheters (2008), 18 descendants of its own
- K981359: GT Leggiero (1999), 14 descendants of its own
- K092396: Spectranetics Quick Cross Extreme Support Catheters (2009), 13 descendants of its own
- K033583: Progreat (2003), 13 descendants of its own

Source page: https://510kreport.com/device/K915414
Methodology: https://510kreport.com/methodology