Catalog Number

S00010

Brand Name

Percussionaire

Version/Model Number

F00012

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

-

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

7763c81f-8295-4f69-8d15-ddcaeef64c4f

Public Version Date

March 12, 2020

Public Version Number

4

DI Record Publish Date

October 21, 2015

Package DI Number

10849436000386

Quantity per Package

1

Contains DI Package

00849436000389

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case