Catalog Number

175-0646-00

Brand Name

ULTRAVIEW SL

Version/Model Number

SUPPLY

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"

Yes

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

K103142

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

c2ab81ef-83b7-440a-ba4b-b0b2b1ae4f5c

Public Version Date

November 10, 2021

Public Version Number

5

DI Record Publish Date

May 31, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-