# K782079: Electrode System, Quik-Prep

- Pathway: 510(k) (Traditional)
- Applicant: Quinton, Inc.
- Decided: Feb 1, 1979 after 50 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.
5 later devices descend from it; 2 cite it directly.
0 of 6 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
- K962115: Cambridge Heart HI-Res Ecg Electrode (1996), 2 descendants of its own
- K023713: Sonoprep Impedance Diagnostics (Idx) System, Model D1000 (2004), 1 descendant of its own
- K013615: Micro-Induction 1000 System (2002), 1 descendant of its own
- K090249: Modification to: Micro-Induction 1000 System (2009), 0 descendants of its own
- K040525: Sonoprep Ultrasonic Skin Permeation System and Topical Anesthetic Kit, Model D2000 (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K782079
Methodology: https://510kreport.com/methodology