Duns Number:026281163
Device Description: A-Tube Pack
Catalog Number
200-0044
Brand Name
AspireAssist A-Tube Pack
Version/Model Number
200-0044
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
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
P150024
Product Code
OYF
Product Code Name
Aspiration Therapy System
Public Device Record Key
c5e1fdba-0e88-4ee3-8a8c-7e8920a69fe1
Public Version Date
October 07, 2019
Public Version Number
4
DI Record Publish Date
July 25, 2016
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2 |
3 | A medical device with high risk that requires premarket approval | 47 |