Duns Number:796986144
Device Description: ACCY 3550-07 ALIGTR CLIP SCREEN CABLE US
Catalog Number
-
Brand Name
N/A
Version/Model Number
3550-07
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
P960009
Product Code
GZB
Product Code Name
STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF)
Public Device Record Key
151366f0-f061-4b4d-b141-64ea577b3769
Public Version Date
July 06, 2018
Public Version Number
2
DI Record Publish Date
April 29, 2018
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 | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |