Catalog Number

P7000

Brand Name

MISTIC

Version/Model Number

P7000

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

-

Prescription Use (Rx)

-

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

373e7ad1-fad7-4a51-b796-dc2eaaa9959f

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

September 17, 2021

Package DI Number

00612223700010

Quantity per Package

6

Contains DI Package

00612223700058

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS