Duns Number:092673953
Device Description: Small Volume Nebulizer Anti-Spill T W/7'Kink Resistant Tubing Standard Connector
Catalog Number
-
Brand Name
Nebulizers
Version/Model Number
1002221
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
K800562,K800562
Product Code
CAF
Product Code Name
Nebulizer (Direct Patient Interface)
Public Device Record Key
5805c481-697c-41bd-8e2d-07038c206b10
Public Version Date
April 08, 2022
Public Version Number
1
DI Record Publish Date
March 31, 2022
Package DI Number
10709078014380
Quantity per Package
50
Contains DI Package
00709078014383
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 746 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 320 |