# K093261: MOVES

- Pathway: 510(k) (Traditional)
- Applicant: Thornhill Research, Inc.
- Decided: Mar 26, 2010 after 158 days
- Product code: BTL (Ventilator, Emergency, Powered (Resuscitator))
- Device class: 2
- Regulation: 21 CFR 868.5925
- Recalls of this device: 2 (2 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K902859 (1991). 63 ancestors in all.
7 later devices descend from it; 2 cite it directly.
4 of 71 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K013931: Omni Oxygen System, Model 1000, Sequal Technologies, Inc. (2002) Summary page 3.
- K052554: Modification to: Ivent 201 Portable Ventilator, Versamed Medical Systems, Inc. (2005) Summary page 3.
- K051476: Uni-Vent Model 73X, Impact Instrumentation, Inc. (2005) Summary page 3.
- K931473: Impact Model 753, Impact Instrumentation, Inc. (1994) Summary page 3.
- K030943: Modification to Hiox, Sensor Medics Corp. (2003) Summary page 3.
- K061435: Medela Vario Suction Pumps, Medela AG (2006) Summary page 3.
- K012059: 8100/8500 Vital Signs Monitor, Criticare Systems, Inc. (2001) Summary page 3.
- K012451: Propaq Encore Models 202, 204, 206; Propaq CS Models 242, 244, 246, Welch Allyn Protocol, Inc. (2001) Summary page 3.

## Most influential descendants
- K141460: Finapres Nova Noninvasive Hemodynamic Monitor (2015), 4 descendants of its own
- K160967: Finapres Nova Noninvasive Hemodynamic Monitor (2017), 3 descendants of its own
- K173916: Finapres Nova Noninvasive Hemodynamic Monitor (2018), 2 descendants of its own
- K140049: Moves SLC (2014), 1 descendant of its own
- K223332: Task Force CORE (2023), 0 descendants of its own

## Recalls of this device
- Nov 19, 2015 · Class I · Z-0586-2016: Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.
- Nov 19, 2015 · Class I · Z-0587-2016: Batteries found unresponsive after storage, not recognized by main device, and are perpetually enabled.

## Indications for use
The MOVESTM is a portable computer controlled electrically powered transport ventilator intended to provide continuous or intermittent emergency ventilatory support for the care of adults who require mechanical ventilation. The MOVESTM is intended to deliver high inspired oxygen concentrations via the MOVESTM 02 mask to spontaneously breathing patients who require elevated inspired oxygen MOVESTM is intended to be used in a transport or emergency setting on adult patients who weigh between 40 and 120kg. MOVESTM provides the following supplemental functions for patients that it is ventilating or to whom it is delivering elevated inspired oxygen: a. Suction The MOVESTM suction pump is intended for aspiration and removal of fluids, tissue (including bone), gases, bodily fluids or infectious materials from wounds or from a patient's airway or respiratory support system. b. Supplementary Oxygen The MOVESTM is intended to provide supplemental oxygen enriched air to patients that require supplemental oxygen. c. Patient Monitoring The MOVESTm is intended to monitor physiological parameters of patients and provide these parameters to a health care provider for interpretation in the form of physiological data and system alarms. Physiological data and system alarms will be available to the care provider from the monitor.

Source page: https://510kreport.com/device/K093261
Methodology: https://510kreport.com/methodology