# K121662: Vecttor VT-200

- Pathway: 510(k) (Abbreviated)
- Applicant: Alan Neuromedical Technologies, LLC
- Decided: Nov 21, 2012 after 169 days
- Product code: LIH (Interferential Current Therapy)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K010565 (2001). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010565: Dynatron STS, Dynatronics Corp. (2001) Summary page 1.

## Most influential descendants
- K231575: Vecttor VT-300 (2024), 0 descendants of its own

## Indications for use
Electrical stimulation delivered by the device is intended for the symptomatic relief of chronic intractable pain and/or management of post-traumatic or post-surgical pain.

Source page: https://510kreport.com/device/K121662
Methodology: https://510kreport.com/methodology