Duns Number:711789789
Catalog Number
-
Brand Name
Single Use Repositionable Clip
Version/Model Number
HX-202LR
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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"
Yes
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
K123601,K123601
Product Code
PKL
Product Code Name
Hemostatic metal clip for the GI tract
Public Device Record Key
139cbc9b-1d25-4e06-a5be-fa6e53ba499b
Public Version Date
February 05, 2021
Public Version Number
4
DI Record Publish Date
September 21, 2016
Package DI Number
14953170385923
Quantity per Package
5
Contains DI Package
04953170385926
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 | 117 |
2 | A medical device with a moderate to high risk that requires special controls. | 1962 |
U | Unclassified | 52 |