# K212977: SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corporation
- Decided: Feb 17, 2022 after 153 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: 1 generation back to K992347 (1999). 1 ancestor in all.
No later device cites it as a predicate yet.
1 of 2 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K992347: Cordis Super Torque MB Angiographic Catheter with Radiopaque Marker Bands, Cordis Corp. (1999) Summary page 4.

## Indications for use
Cordis Angiographic Catheters with Marker Bands are designed to provide angiographic visualization and linear measurement of the vasculature when combined with the delivery of radiopaque contrast media to selected sites in the vascular system.

Source page: https://510kreport.com/device/K212977
Methodology: https://510kreport.com/methodology