Duns Number:481233849
Device Description: AIR-FLOW® handy 3.0
Catalog Number
FT-220#NA/006
Brand Name
AIR-FLOW
Version/Model Number
B
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"
-
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
K132478
Product Code
EFB
Product Code Name
Handpiece, Air-Powered, Dental
Public Device Record Key
df226813-dc1c-4d6f-aa9e-17900fbfff1a
Public Version Date
July 28, 2022
Public Version Number
1
DI Record Publish Date
July 20, 2022
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 | 226 |
2 | A medical device with a moderate to high risk that requires special controls. | 422 |
3 | A medical device with high risk that requires premarket approval | 11 |