Catalog Number

-

Brand Name

Circulaire

Version/Model Number

0296

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

Yes

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

K926055,K926055

Product Code

BYG

Product Code Name

Mask, Oxygen

Public Device Record Key

b6f1b5a0-6513-4060-b434-eb7cd15ea57b

Public Version Date

September 08, 2020

Public Version Number

1

DI Record Publish Date

August 31, 2020

Package DI Number

10709078009140

Quantity per Package

50

Contains DI Package

00709078009143

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-