Duns Number:149818952
Catalog Number
406427
Brand Name
SJM™
Version/Model Number
406427
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
K884494,K884494
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
66bb19b5-1261-40fa-9423-7330a1ae1b25
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 15, 2015
Package DI Number
15415067009446
Quantity per Package
10
Contains DI Package
05415067009449
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 70 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1429 |
| 3 | A medical device with high risk that requires premarket approval | 736 |