# K982770: 6F Envoy Guiding Catheter

- Pathway: 510(k) (Special)
- Applicant: Cordis Corp.
- Decided: Aug 18, 1998 after 26 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.
1 later device descends from it; 1 cites it directly.
0 of 2 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 VISTA BRITE TIP Guiding Catheter: named in the summary without a submission number
- (no number) Cordis Endovascular Systems, Inc. ENVOY Guiding Catheter: named in the summary without a submission number

## Most influential descendants
- K112828: Revive Intermediate Catheter (Revive IC) (2011), 0 descendants of its own

## Indications for use
The VISTA BRITE TIP and ENVOY Guiding Catheters are intended for use for intravascular introduction of interventional/diagnostic devices into the coronary, peripheral, and neuro vasculature.

Source page: https://510kreport.com/device/K982770
Methodology: https://510kreport.com/methodology