Catalog Number

9028-0010-01

Brand Name

Compumedics Grael

Version/Model Number

Grael LT

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

K093223,K093223

Product Code

GWQ

Product Code Name

Full-Montage Standard Electroencephalograph

Public Device Record Key

e42641a1-1c97-4425-9fb1-b455f6b6dd75

Public Version Date

April 27, 2021

Public Version Number

4

DI Record Publish Date

December 22, 2016

Package DI Number

09342451001887

Quantity per Package

5

Contains DI Package

09342451001832

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box