Duns Number:025460908
Device Description: NEBULIZER,KIT,T-MOUTHPIECE,7 TUBE,SC
Catalog Number
HCS4482VA
Brand Name
Medline
Version/Model Number
HCS4482VA
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
Product Code
CAF
Product Code Name
Nebulizer (direct patient interface)
Public Device Record Key
db189ec7-0601-4a95-9dcf-63ddb97ddede
Public Version Date
April 05, 2022
Public Version Number
2
DI Record Publish Date
July 14, 2021
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 | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |