# K962759: 4F Nylex Angiographic Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cordis Corp.
- Decided: Oct 10, 1996 after 86 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.
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. The FDA summary names its predicate without a number.
- (no number) Cordis Corporation 4F Nylex Angiographic Catheter: named in the summary without a submission number
- (no number) Cordis Corporation 4F Infiniti Angiographic Catheter: named in the summary without a submission number

## Most influential descendants
- K971646: 4F Nylex Angiography Catheter/5F Nylex Angiography Catheter (1997), 1 descendant of its own
- K181836: 4F Infiniti Angiographic Catheter, 4F & 5F Nylex Angiography Catheters, 4F & 5F Tempo Angiography Catheters (2018), 0 descendants of its own

## Indications for use
The Cordis 4F Nylex Angiographic Catheters are intended for the delivery of radiopaque contrast medium to selected sites in the vasculature.

Source page: https://510kreport.com/device/K962759
Methodology: https://510kreport.com/methodology