# K971914: Teca NCS Electrode System 2000

- Pathway: 510(k) (Traditional)
- Applicant: Medelec, Inc. D.B.A. Teca Corp.
- Decided: Mar 26, 1998 after 307 days
- Product code: GXY (Electrode, Cutaneous)
- Device class: 2
- Regulation: 21 CFR 882.1320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have 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
- K062198: Sunspots Pre-Gelled Surface Electrodes (2006), 6 descendants of its own
- K110289: Friendship Medical Disposable Pre-Gelled AG / Agcl Surface Electrode (2011), 2 descendants of its own
- K073532: Disposable Adhesive Surface Electrodes, Disc Electrodes (2008), 2 descendants of its own
- K142159: Disposable Pre-Gelled Surface Electrode (2015), 1 descendant of its own
- K081871: Universal Electrodes (2008), 1 descendant of its own

## Indications for use
The NCS Electrode System 2000 is for electromyographic recording, stimulating, and referencing in motor, sensory nerve conduction, and volitional electromyography.

Source page: https://510kreport.com/device/K971914
Methodology: https://510kreport.com/methodology