Duns Number:333710619
Device Description: This is a medical device.
Catalog Number
N.A.
Brand Name
PIEZOsoft
Version/Model Number
1.009.8488
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K080089
Product Code
ELC
Product Code Name
Scaler, ultrasonic
Public Device Record Key
2b645101-6ef9-4f65-8502-77583e4b702c
Public Version Date
November 08, 2021
Public Version Number
4
DI Record Publish Date
November 02, 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 | 194 |
2 | A medical device with a moderate to high risk that requires special controls. | 153 |