Duns Number:005473608
Device Description: REVOTEK LC™ Intro Package, B2 (1 x Putty Stick, 1 x Lightproof storage case, 1 x GC Spatul REVOTEK LC™ Intro Package, B2 (1 x Putty Stick, 1 x Lightproof storage case, 1 x GC Spatula N° 2)
Catalog Number
001842
Brand Name
REVOTEK LC™
Version/Model Number
001842
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
K012542
Product Code
LBH
Product Code Name
VARNISH, CAVITY
Public Device Record Key
46ad70fd-769d-4bb9-9d2f-4bb1cc8e3071
Public Version Date
August 15, 2022
Public Version Number
1
DI Record Publish Date
August 05, 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 | 480 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4772 |