Clinical Movement Analysis Society of UK and Ireland:CMAS Home Page
CMAS was formed to encourage professional interaction, develop and monitor professional standards and training and to stimulate and advance scientific knowledge in the fields of clinical motion analysis.
- CMAS Standards - April 2004 This document details the standards developed by the Standards Working Group of CMAS.
Commission for Motion Laboratory Accreditation, Inc. (USA):CMLA Home Page
CMLA is a nonprofit organization established and operated to enhance the clinical care of persons with disorders of human motion by evaluating and accrediting clinical motion laboratories by a set of standard criteria.
Standard Assessment of Motion System Accuracy:GCMAS-SAMSA
The GCMAS Standards Committee has proposed a protocol for quantifying the accuracy of a motion analysis system (i.e., how accurate the system is at locating markers). This protocol is intended to test video-based systems that employ reflective markers, though it is possible that it could be used to test systems with active markers as well. SAMSA uses a simple device based on a earlier design used by Jim Richards to compare motion systems.
- Device Plans
- Paper "A proposed standard for assessing the marker-location accuracy of video-based motion analysis systems"
- Action Technology - Motorredutores
FMS - Hugh Williamson Gait Analysis Laboratory (AU):
- FMS Brochure "The Functional Mobility Scale - Escala de Mobilidade Funcional (2ª versão)"
Electromyography System: FDA 510(k)
Regulation Number: 890.1375
U.S. Food and Drug Administration
Subpart B--Physical Medicine Diagnostic Devices
Sec. 890.1375 Diagnostic electromyograph.
(a)Identification. A diagnostic electromyograph is a device intended for medical purposes, such as to monitor and display the bioelectric signals produced by muscles, to stimulate peripheral nerves, and to monitor and display the electrical activity produced by nerves, for the diagnosis and prognosis of neuromuscular disease.
(b)Classification. Class II (performance standards).
Regulation Number: 882.5050
Subpart F--Neurological Therapeutic Devices
Sec. 882.5050 Biofeedback device.
(a)Identification. A biofeedback device is an instrument that provides a visual or auditory signal corresponding to the status of one or more of a patient's physiological parameters (e.g., brain alpha wave activity, muscle activity, skin temperature, etc.) so that the patient can control voluntarily these physiological parameters.
(b)Classification. Class II (special controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter when it is a prescription battery powered device that is indicated for relaxation training and muscle reeducation and prescription use, subject to 882.9.
Banco de Dados:
- Exemplo (1) Cadastro do Paciente, (2) Histórico, (3) Biomecânica, (4) Exame Físico