# K020890: Spyglass 4 FR Angiographicy Catheter

- Pathway: 510(k) (Special)
- Applicant: St Jude Medical
- Decided: Apr 17, 2002 after 29 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. The FDA summary names its predicate without a number.
- (no number) Spyglass™ 6Fr & 5Fr Angiographic Catheters: named in the summary without a submission number

## Indications for use
Spyglass™ Angiographic Catheters are designed for delivery of radiopaque contrast media during angoigraphic procedures.

Source page: https://510kreport.com/device/K020890
Methodology: https://510kreport.com/methodology