# K960721: Paceart Wrist Electrodes

- Pathway: 510(k) (Traditional)
- Applicant: Paceart, Inc.
- Decided: Jul 18, 1996 after 147 days
- Product code: DRX (Electrode, Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2360
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) Medtronic 9427 Wrist Electrode: named in the summary without a submission number

## Indications for use
Paceart Wrist Electrodes are intended to be used for home monitoring of pacemaker patients via telephone monitoring systems.

Source page: https://510kreport.com/device/K960721
Methodology: https://510kreport.com/methodology