# K993934: V Quick Patch

- Pathway: 510(k) (Traditional)
- Applicant: Vq Corp.
- Decided: Aug 15, 2000 after 271 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) Electrocardiograph electrodes: named in the summary without a submission number
- (no number) K-Snap, Silver/Silver Chloride ECG electrodes: named in the summary without a submission number
- (no number) Fastrace® Tab ECG Electrodes: named in the summary without a submission number
- (no number) Q Trace: named in the summary without a submission number

## Indications for use
The V Quick Patch System is intended to be used as an electrocardiograph electrode and a placement device for the placement of electrocardiograph electrodes.

Source page: https://510kreport.com/device/K993934
Methodology: https://510kreport.com/methodology