Catalog Number

-

Brand Name

HyperView

Version/Model Number

103-A001

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

K161237

Product Code

MUD

Product Code Name

Oximeter, Tissue Saturation

Public Device Record Key

57db2f50-3e09-4857-8954-34eb0fd919e5

Public Version Date

July 06, 2018

Public Version Number

3

DI Record Publish Date

November 23, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-