Catalog Number

P5-TA

Brand Name

Percussionaire

Version/Model Number

P5-TA

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

K905236,K905236,K905236

Product Code

NHJ

Product Code Name

Device, Positive Pressure Breathing, Intermittent

Public Device Record Key

d99789d3-bfe8-43fc-9d78-916b6de85e39

Public Version Date

October 24, 2022

Public Version Number

4

DI Record Publish Date

December 03, 2018

Package DI Number

20849436000536

Quantity per Package

5

Contains DI Package

00849436000532

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case