Natus 085-458000

Trade name

Natus

Generic name

Electromyograph

Model / reference

085-458000

Primary DI / UDI-DI

00382830059435

FDA product code

GWF

GMDN term

Electromyograph

Device class

Class II

Regulation number

882.1870

GUDID distribution status

In Commercial Distribution

Category: Electromyograph

Other devices filed under FDA product code GWF (Stimulator, Electrical, Evoked Response).

• 533637 by inomed Medizintechnik GmbH
• Carefusion Nicolet EDX by Carefusion 209, Inc.
• NIHON KOHDEN NEUROPACK SIGMA MEB-5500A EVOKED RESPONSE & EMG MEASURING SYSTEM by NIHON KOHDEN AMERICA, INC.
• Pediguard Nerve Detector System by Spine Vision, Inc.
• MEB-2300A Neuropack Evoked Potential and EMG Measuring System by Nihon Kohden Corp.
• 530627 by inomed Medizintechnik GmbH
• NEUROVISION JJB SYSTEM by Nuvasive, Inc.
• Magstim Rapid by Magstim Corporation US
• ST10 Progr. Evoked Response Stimulator by Teca, Inc.
• High Speed Magnetic Stimulator by Cadwell Laboratories, Inc.

• Natus Neurology S-Mjt-7522-Ll

  Class II

  FDA 510(k) K973444 Active Cleared 20 Nov 1997 GUDID on market

• Natus Neurology S-019-400500

  Class II

  FDA 510(k) K850108 Active Cleared 11 Apr 1985 GUDID on market

• Natus Neurology S035K020

  Class II

  FDA 510(k) K965065 Active Cleared 20 Jun 1997 GUDID on market

• Natus 482-649300

  Class II

  FDA 510(k) K991054 Active Cleared 3 Nov 1999 GUDID on market

See all devices from Natus Neurology Incorporated →