Catalog Number

NC01-030/03

Brand Name

NEUROCAP

Version/Model Number

3.0 mm

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Safe

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

K152684

Product Code

JXI

Product Code Name

Cuff, Nerve

Public Device Record Key

6bd2ae9b-91d1-4a8e-b78b-07594590d3cf

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

February 02, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-