Catalog Number

A50096-D

Brand Name

Percussionaire

Version/Model Number

A50096-D

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"

-

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

K905235,K905235

Product Code

CBK

Product Code Name

Ventilator, Continuous, Facility Use

Public Device Record Key

1f4f0144-ac75-48e4-8894-bd9f7cafb404

Public Version Date

October 24, 2022

Public Version Number

6

DI Record Publish Date

May 26, 2016

Package DI Number

10849436000294

Quantity per Package

5

Contains DI Package

00849436000297

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case