Catalog Number

501-00046-01

Brand Name

NESS L300-Plus System

Version/Model Number

L3P-4100

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 30, 2017

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

IPF

Product Code Name

Stimulator, muscle, powered

Public Device Record Key

4f37d361-c9bd-48bf-9dfb-420e0fead218

Public Version Date

September 20, 2021

Public Version Number

5

DI Record Publish Date

February 02, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-