Duns Number:185432994
Device Description: ENTRAINMENT NEBULIZER,BARREL STANDARD FLOW UP TO 12LPM, LONG TUBE, AIRLIFE FIT
Catalog Number
P3000NCC-L
Brand Name
CURAPLEX
Version/Model Number
301-P3000NCF-L
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
K893942,K893942
Product Code
CAF
Product Code Name
Nebulizer (Direct Patient Interface)
Public Device Record Key
d2515c31-eae5-4bbe-953f-b462e60dedf1
Public Version Date
June 10, 2022
Public Version Number
2
DI Record Publish Date
September 15, 2021
Package DI Number
00612223030124
Quantity per Package
40
Contains DI Package
00612223030131
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 6 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 47 |