Catalog Number

P3000NCC

Brand Name

CURAPLEX

Version/Model Number

301-P3000NCF

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"

Yes

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

K893942,K893942

Product Code

CAF

Product Code Name

Nebulizer (Direct Patient Interface)

Public Device Record Key

9c7b9271-0807-4209-a31a-b3515f20ddd9

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 15, 2021

Package DI Number

00612223030100

Quantity per Package

40

Contains DI Package

00612223030117

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS