Catalog Number
045057
Brand Name
MyOcclude
Version/Model Number
045057
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
K964251,K964251
Product Code
DXC
Product Code Name
CLAMP, VASCULAR
Public Device Record Key
12bb8198-e250-40fd-a330-bacfc638d729
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
September 24, 2016
Package DI Number
20884521051161
Quantity per Package
12
Contains DI Package
10884521051164
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 132 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8540 |
| 3 | A medical device with high risk that requires premarket approval | 202 |
| U | Unclassified | 40 |