# K024071: Guidant Syncrus Internal Cardioversion System

- Pathway: 510(k) (Special)
- Applicant: Guidant Corporation, Cardiac Surgery
- Decided: Feb 14, 2003 after 66 days
- Product code: NHW (Electrode, Pacing And Cardioversion, Temporary, Epicardial)
- 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
Longest line of descent: 2 generations back to K800937 (1980). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020701: Syncrus Internal Cardioversion System, Guidant Corporation, Cardiac Surgery (2002) Summary page 2.

## Indications for use
The Guidant SYNCRUS™ Internal Cardioversion System is indicated for use in post-operative cardiac surgery patients who require temporary atrial or ventricular pacing/sensing and/or atrial cardioversion.

Source page: https://510kreport.com/device/K024071
Methodology: https://510kreport.com/methodology