Duns Number:316483072
Catalog Number
-
Brand Name
Temporary CB A3
Version/Model Number
FLTCA301US
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
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
K193553,K193553
Product Code
EBG
Product Code Name
Crown And Bridge, Temporary, Resin
Public Device Record Key
e6c747bf-9a16-4664-b594-09e427b2b60d
Public Version Date
October 29, 2021
Public Version Number
2
DI Record Publish Date
September 24, 2020
Package DI Number
EBGOFLTCA301US2
Quantity per Package
1
Contains DI Package
EBGOFLTCA301US1
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 89 |