Catalog Number

-

Brand Name

Pneupac

Version/Model Number

530A1167NONEU

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

K123957

Product Code

BTL

Product Code Name

Ventilator, emergency, powered (resuscitator)

Public Device Record Key

720a39ac-3119-4ef7-93bb-a98f5dc96c90

Public Version Date

January 29, 2021

Public Version Number

3

DI Record Publish Date

August 01, 2019

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-