Catalog Number

-

Brand Name

STIMULATOR PROBE POD (MCI

Version/Model Number

70921661

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

June 01, 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

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

K923056

Product Code

ETN

Product Code Name

STIMULATOR, NERVE

Public Device Record Key

9e37d4e6-64e3-43f1-9bc2-0feee9896788

Public Version Date

October 06, 2022

Public Version Number

5

DI Record Publish Date

May 11, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-