Duns Number:022721133
Device Description: Nebulizer Tee Adaptor, Anti-drool 22 mm (I.D.) x 22 mm (O.D.) x 18 mm (I.D.), for use with Nebulizer Tee Adaptor, Anti-drool 22 mm (I.D.) x 22 mm (O.D.) x 18 mm (I.D.), for use with Salter Labs® Nebulizers.
Catalog Number
8910-0
Brand Name
n/a
Version/Model Number
8910-0
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K962879,K962879
Product Code
CCQ
Product Code Name
NEBULIZER, MEDICINAL, NON-VENTILATORY (ATOMIZER)
Public Device Record Key
dbe62fc3-2eed-4bd0-9c6b-9b5145831d07
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
November 30, 2016
Package DI Number
10607411890144
Quantity per Package
50
Contains DI Package
00607411890147
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 | 865 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1134 |