# K180082: geko T-2 and geko Plus R-2

- Pathway: 510(k) (Traditional)
- Applicant: Firstkind, Ltd.
- Decided: Feb 11, 2018 after 31 days
- Product code: IPF (Stimulator, Muscle, Powered)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K872976 (1987). 7 ancestors in all.
4 later devices descend from it; 3 cite it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K162987: FA100 SCCD (Sequential Continuous Contraction Device), Flowaid Medical Technologies, Corp (2017) Summary page 4.

## Most influential descendants
- K193045: geko™ W-2 (2020), 1 descendant of its own
- K181059: geko T-3 Neuromuscular Stimulator (2018), 1 descendant of its own
- K212762: geko W-2 (2021), 0 descendants of its own
- K191113: geko T-2 and geko T-3 Neuromuscular Stimulators (2019), 0 descendants of its own

## Indications for use
• Increasing local blood circulation • Immediate post-surgical stimulation of the calf muscles to prevent venous thrombosis • Edema reduction

Source page: https://510kreport.com/device/K180082
Methodology: https://510kreport.com/methodology