# K162987: FA100 SCCD (Sequential Continuous Contraction Device)

- Pathway: 510(k) (Traditional)
- Applicant: Flowaid Medical Technologies, Corp
- Decided: Feb 14, 2017 after 110 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: 2 generations back to K872976 (1987). 6 ancestors in all.
5 later devices descend from it; 1 cites 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)
- K050046: Rehabilicare IF 3 Wave Interferential Stimulator System, Model 7110S, Compex Technologies, Inc. (2005) Summary page 4.

## Most influential descendants
- K180082: geko T-2 and geko Plus R-2 (2018), 4 descendants of its own
- 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 calf muscles to prevent venous thrombosis Preventing or retarding disuse atrophy Edema reduction

Source page: https://510kreport.com/device/K162987
Methodology: https://510kreport.com/methodology