Catalog Number

90519B

Brand Name

Blease

Version/Model Number

BLEASE

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 16, 2018

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

K903702

Product Code

DQA

Product Code Name

Oximeter

Public Device Record Key

1cfa9996-4580-42c2-8e88-0e24029c23dc

Public Version Date

July 06, 2018

Public Version Number

4

DI Record Publish Date

November 10, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-