# K051561: Asahi Angiographic Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Asahi Intecc Co., Ltd.
- Decided: Nov 2, 2005 after 142 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
Longest line of descent: 3 generations back to K921310 (1992). 5 ancestors in all.
2 later devices descend from it; 1 cites it directly.
1 of 8 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K960975: 1-4F Infiniti Angiographic Catheter, Cordis Corp. (1996) Summary page 1.
- K970854: 5 FR  and 6 FR Infiniti Angiographic Catheter, Cordis Corp. (1997) Summary page 1.
- K862006: Stand & High Flow Femoral-Ventricular Pigtail Cath, Cordis Corp. (1986) Summary page 1.

## Most influential descendants
- K082559: Spectranetics Cross-Pilot Turbo Elite Support Catheter (2008), 1 descendant of its own
- K090913: Cross-Pilot Turbo Elite Support Catheter (2009), 0 descendants of its own

## Indications for use
The Asahi Angiographic Catheters are indicated for the delivery of radiopaque contrast medium to selected sites in the vascular system.

Source page: https://510kreport.com/device/K051561
Methodology: https://510kreport.com/methodology