Duns Number:371618773
Device Description: MDMG-5221 CB
Catalog Number
K9300521B
Brand Name
Barco Mammo Tomosynthesis
Version/Model Number
MDMG-5221
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
K103792
Product Code
LLZ
Product Code Name
System, image processing, radiological
Public Device Record Key
e2e1d2a1-4666-4233-87f1-bc04a757e2be
Public Version Date
December 20, 2018
Public Version Number
4
DI Record Publish Date
August 19, 2016
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 | 105 |
2 | A medical device with a moderate to high risk that requires special controls. | 259 |