Catalog Number

875-NK

Brand Name

Rescuer Emergency CPAP with Medium CPAP Mask

Version/Model Number

8705-NK

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

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

K122610,K122610

Product Code

BYE

Product Code Name

Attachment, Breathing, Positive End Expiratory Pressure

Public Device Record Key

4e5c2e67-7a79-486f-8f6c-3ec824edfb63

Public Version Date

January 14, 2020

Public Version Number

1

DI Record Publish Date

January 06, 2020

Package DI Number

B0028705NK1

Quantity per Package

6

Contains DI Package

B0028705NK0

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case