# K070926: Electrode/Extension Cables, Models Atar

- Pathway: 510(k) (Special)
- Applicant: Oscor, Inc.
- Decided: Jun 7, 2007 after 65 days
- Product code: IKD (Cable, Electrode)
- Device class: 2
- Regulation: 21 CFR 890.1175
- Recalls of this device: 2 (2 Class I)
- 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.
1 of 2 devices in its family (counting itself) has 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.

## Most influential descendants
- K200674: AtriAmp, AtriAmp - Pacing Cable Medtronic Connector, AtriAmp - Pacing Cable Oscor Connector (2020), 0 descendants of its own

## Recalls of this device
- Mar 31, 2017 · Class I · Z-2733-2017: The Reusable Oscor ATAR extension cables could separate from the connector during use.
- Mar 31, 2017 · Class I · Z-2340-2017: The Reusable Oscor ATAR extension cables could separate from the connector during use.

## Indications for use
Electrode/extension cable is intended to connect an electrode/lead from a patient or another cable to a diagnostic machine or an external pacemaker.

Source page: https://510kreport.com/device/K070926
Methodology: https://510kreport.com/methodology