# K160299: geko (TM) Plus R-2 Neuromuscular Stimulator

- Pathway: 510(k) (Special)
- Applicant: Firstkind Limited
- Decided: Apr 8, 2016 after 64 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: 4 generations back to K880235 (1988). 4 ancestors in all.
1 later device descends from it; 1 cites 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)
- K152677: geko T-2 Neuromuscular Stimulator, Firstkind Limited (2015) Summary page 4.

## Most influential descendants
- K163125: geko™ T-2 and geko™ Plus R-2 Neuromuscular Stimulators (2017), 0 descendants of its own

## Indications for use
The geko(TM) Plus R-2 is intended for: - Increasing local blood circulation; and - Immediate post-surgical stimulation of the calf muscles to prevent venous thrombosis.

Source page: https://510kreport.com/device/K160299
Methodology: https://510kreport.com/methodology