Duns Number:550888712
Device Description: This unit operates on standard AC power. Treatments are delivered quickly, safely, and con This unit operates on standard AC power. Treatments are delivered quickly, safely, and conveniently, making this unit ideal for all ages.This nebulizer should be used under the supervision of a licensed physician and/or a respiratory therapist. With you physician and/or respiratory therapist, you will feel comfortable and confident knowing that you are obtaining the most effective inhalation treatments for your respiratory condition.
Catalog Number
-
Brand Name
Nebulizer(direct patient interface)
Version/Model Number
WHQ-1902WH(408D)
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
K003344
Product Code
CAF
Product Code Name
Nebulizer (Direct Patient Interface)
Public Device Record Key
738b49ab-68c3-4f51-92b2-81748cfd439d
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
July 16, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1 |