Musculoskeletal Evaluation Technologies for Chiropractic and Physical Medicine
Surface Electromyography (SEMG)Surface Electromyography (SEMG)Muscle TestingDynamic Range of Motion (DROM)Dynamic Range of Motion (DROM)
Neuromuscular and EMG Products Neuromuscular and EMG Learning Center Certifications Testimonials
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Certifications

Questions? Comments? Contact us online or call 800-426-0316.

Myotronics-Noromed, Inc. manufacturers FDA registration number: 3014732

All Noromed devices are registered with the U.S. Food and Drug Administration and have received permission for marketing under 510(k) pre-market notifications.

Dates and FDA document control numbers for all instruments are listed below:

Item 510(k) Number Date Cleared
Norotrack 360 K920690 05-20-92
Norodyn 2000 K922838A 09-02-94
Norodyn 8000 (Physiotech 4000) K922270 09-02-94
Norodyn 8000 (Spectral analysis) K992439 08-13-99
MES-9000/Norotrack 360 System K013357 11-08-01
MES-9000/EMG System K013399 11-13-01

ISO INFORMATION

Since 1998 Myotronics-Noromed's Quality Systems have been continually audited and approved by independent auditors authorized by the International Standards Organization (ISO). All major products meet the additional safety and efficacy requirements of that organization which permit affixing the "CE" mark.

QUALITY POLICY

Myotronics-Noromed, Inc. is committed to manufacturing quality products, backed by strong service support, that satisfy customer requirements. Products are designed and manufactured to meet current legal and regulatory standards. To insure a high level of customer satisfaction, the Company maintains a quality system designed to actively monitor and continually improve its products, services and the quality system itself.