Catalog Number

-

Brand Name

Roscoe Medical

Version/Model Number

50018

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 07, 2019

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

-

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

8b3acce8-f3ef-4593-93aa-a31fdecb2e6e

Public Version Date

May 08, 2019

Public Version Number

3

DI Record Publish Date

October 07, 2016

Package DI Number

80092237603181

Quantity per Package

2

Contains DI Package

60092237603187

Package Discontinue Date

May 07, 2019

Package Status

Not in Commercial Distribution

Package Type

CA