# K092118: Angiographic Catheter, Model Angios

- Pathway: 510(k) (Traditional)
- Applicant: Oscor, Inc.
- Decided: Jan 13, 2010 after 183 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.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The model Angios angiographic catheters are designed to be used for delivering radiopaque media to selected sites in the vascular system in conjunction with routine diagnostic procedure.

Source page: https://510kreport.com/device/K092118
Methodology: https://510kreport.com/methodology