# K021088: Joguide Cardiovascular Guiding C Atheter

- Pathway: 510(k) (Special)
- Applicant: Jomed Catheter, Inc.
- Decided: May 2, 2002 after 28 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- 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 JOMED Guiding Catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.

Source page: https://510kreport.com/device/K021088
Methodology: https://510kreport.com/methodology