Duns Number:006261481
Device Description: INTRO 6212BTK-5 5PK 12FR
Catalog Number
-
Brand Name
SOLO-TRAK®-KR
Version/Model Number
6212BTK-5
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 25, 2019
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
K965167,K965167
Product Code
DYB
Product Code Name
INTRODUCER, CATHETER
Public Device Record Key
75544d0c-1722-4371-81f9-1bc6eef1628b
Public Version Date
June 07, 2019
Public Version Number
5
DI Record Publish Date
January 03, 2017
Package DI Number
10681490143735
Quantity per Package
5
Contains DI Package
00681490143738
Package Discontinue Date
January 25, 2019
Package Status
Not in Commercial Distribution
Package Type
PK
| 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 |