Duns Number:018493531
Device Description: Software Upgrade Kit
Catalog Number
15211-01
Brand Name
C7-XR™
Version/Model Number
C.0.4 Software Upgrade
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
-
Product Code
NQQ
Product Code Name
SYSTEM, IMAGING, OPTICAL COHERENCE TOMOGRAPHY (OCT)
Public Device Record Key
fb6bc945-02b7-4442-913e-2af0a5b7f94e
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
March 18, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 25 |