Duns Number:657263687
Catalog Number
-
Brand Name
PIEZO ELECTRIC ULTRASONIC SCALER(LED)
Version/Model Number
ART-P6
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K071981
Product Code
ELC
Product Code Name
Scaler, Ultrasonic
Public Device Record Key
25a69748-50ef-4bc4-9289-a4f1a6e8e59c
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
January 19, 2017
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 | 5 |
2 | A medical device with a moderate to high risk that requires special controls. | 131 |