Catalog Number

-

Brand Name

N/A

Version/Model Number

8225825

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

Yes

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

K934426,K934426

Product Code

ETN

Product Code Name

STIMULATOR, NERVE

Public Device Record Key

067da8a2-c55e-46f6-a88c-4a2bef47f6b6

Public Version Date

March 04, 2021

Public Version Number

2

DI Record Publish Date

April 04, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-