Catalog Number

-

Brand Name

L100 Go System

Version/Model Number

LG1-5Y00

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GZI

Product Code Name

STIMULATOR, NEUROMUSCULAR, EXTERNAL FUNCTIONAL

Public Device Record Key

510dd143-940b-49d5-a862-20d992f5939d

Public Version Date

April 30, 2020

Public Version Number

1

DI Record Publish Date

April 22, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-