# K063872: Kinesia

- Pathway: 510(k) (Traditional)
- Applicant: Cleveland Medical Devices, Inc.
- Decided: Apr 6, 2007 after 98 days
- Product code: GYD (Transducer, Tremor)
- Device class: 2
- Regulation: 21 CFR 882.1950
- 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 K854030 (1986). 8 ancestors in all.
10 later devices descend from it; 1 cites it directly.
0 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042039: Family of Crystal 20 Monitors Model #CS20-600,900,1300,1400,2400 & 120, Cleveland Medical Devices, Inc. (2004) Summary page 1.
- K010270: Tremorometer, Flexable Systems, Inc. (2001) Summary page 1.
- K991033: Actiwatch-Score, Mini-Mitter Co., Inc. (1999) Summary page 1.

## Most influential descendants
- K140086: Personal Kinetigraph (PKG) System (2014), 9 descendants of its own
- K213519: Rune Labs Tremor Transducer System (2022), 4 descendants of its own
- K220820: Parky App (2022), 3 descendants of its own
- K161717: Personal Kinetigraph (PKG) System (2016), 3 descendants of its own
- K250153: Neu Platform (2025), 1 descendant of its own

## Indications for use
Kinesia is intended to monitor physical motions and muscle activity to quantify kinematics of movement disorder symptoms such as tremor and assess activity in any instance where quantifiable analysis of motion and muscle activity is desired.

Source page: https://510kreport.com/device/K063872
Methodology: https://510kreport.com/methodology