Catalog Number

-

Brand Name

Cascade IOMAX Intraoperative Monitor

Version/Model Number

199305-200

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K162199

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

e3255da7-e782-4c0d-a840-f9cacecd8670

Public Version Date

July 30, 2019

Public Version Number

2

DI Record Publish Date

July 09, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-