Catalog Number

A50474-2D

Brand Name

Percussionaire

Version/Model Number

A50474-2D

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 05, 2022

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

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

K905236,K905236

Product Code

NHJ

Product Code Name

Device, Positive Pressure Breathing, Intermittent

Public Device Record Key

6916ac03-9b24-46d8-93ff-f4137a0e2d6e

Public Version Date

October 24, 2022

Public Version Number

6

DI Record Publish Date

October 21, 2015

Package DI Number

10849436000324

Quantity per Package

5

Contains DI Package

00849436000327

Package Discontinue Date

August 05, 2022

Package Status

Not in Commercial Distribution

Package Type

-