# K973298: Cardima Vueport Coronary Sinus Balloon Occlusion Guiding Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Cardima, Inc.
- Decided: Jun 26, 1998 after 297 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.
60 later devices descend from it; 5 cite it directly.
0 of 61 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) Electro-Catheter Corp., Elecath Occlusion Catheter: named in the summary without a submission number

## Most influential descendants
- K021284: Easytrak Guiding Catheter (2002), 26 descendants of its own
- K041151: Kerberos Occluding Guide Catheter and Accessories (2004), 25 descendants of its own
- K021455: Rapido Guiding Catheter, 6F Model# 6776; Rapido Guiding Catheter, 8F Model# 6775, 6777, 6778, 6779, 6780, 6781, 6782, (2002), 25 descendants of its own
- K080987: Bridgepoint Medical Stingray Device and Accessories (2009), 24 descendants of its own
- K031505: Rapido Cut-Away Guiding Catheter (2003), 21 descendants of its own

## Indications for use
The VUEPORT is intended for use to access the coronary sinus and perform occlusive venograms. The catheter may serve as a conduit for the delivery and support of other devices.

Source page: https://510kreport.com/device/K973298
Methodology: https://510kreport.com/methodology