MYOLAB II - The Myolab II was specifically designed for use - MOTION CONTROL, INC

Duns Number:177661386

Device Description: The Myolab II was specifically designed for use in fitting and troubleshooting the Utah Ar The Myolab II was specifically designed for use in fitting and troubleshooting the Utah Arm and ProPlus myoelectric prostheses. It can be used to locate muscle activity down to 0.2 microvolts in the remnant limb. The adjustable gain feature allows the device to test and train muscle EMG for any single or dual-channel myoelectric control system.

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More Product Details

Catalog Number

-

Brand Name

MYOLAB II

Version/Model Number

MC-200

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

HCC

Product Code Name

Device, Biofeedback

Device Record Status

Public Device Record Key

9e98b82a-2b0d-4296-8be3-6522083c4e60

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 04, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MOTION CONTROL, INC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 1