# K930069: Bipolar Balloon Pacing Catheter by J-Lloyd

- Pathway: 510(k) (Traditional)
- Applicant: J-Lloyd Medical, Inc.
- Decided: Jan 28, 1994 after 387 days
- Product code: LDF (Electrode, Pacemaker, Temporary)
- Device class: 2
- Regulation: 21 CFR 870.3680
- 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; 2 cite 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K973639: Electrode Semi-Flotation Catheter by J-Lloyd Medical, Inc. (1998), 0 descendants of its own
- K971504: Hexapolar Electrode Balloon Flotation Catheter (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K930069
Methodology: https://510kreport.com/methodology