Duns Number:957536014
Device Description: Superficial Peroneal Biosensor (Right) Individual
Catalog Number
-
Brand Name
ADVANCE
Version/Model Number
NC-S33
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
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
K041320,K041320
Product Code
JXE
Product Code Name
Device, Nerve Conduction Velocity Measurement
Public Device Record Key
895bcf90-d465-44da-9426-cab4741705aa
Public Version Date
October 22, 2018
Public Version Number
4
DI Record Publish Date
September 07, 2016
Package DI Number
10851221006114
Quantity per Package
6
Contains DI Package
00851221006117
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 31 |