Catalog Number

-

Brand Name

NA

Version/Model Number

E-NMT-01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K051635

Product Code

KOI

Product Code Name

STIMULATOR, NERVE, PERIPHERAL, ELECTRIC

Public Device Record Key

04a31a5c-dba2-45d7-a6ae-99f3fbe48c2b

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

May 20, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-