Catalog Number

80-4788

Brand Name

CorticaLINK MI

Version/Model Number

80-4788

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

-

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

HWN

Product Code Name

Instrument, Compression

Public Device Record Key

cf4b977f-c5cc-4d2a-ae8d-a2deaeb07df4

Public Version Date

November 28, 2018

Public Version Number

3

DI Record Publish Date

April 24, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-