Duns Number:627879687
Device Description: The Histolock resection device is an electrosurgical device designed to be used to endosco The Histolock resection device is an electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during Gastrointestinal (GI) endoscopic procedures.
Catalog Number
00711871
Brand Name
Histolock
Version/Model Number
00711871
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
March 31, 2020
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"
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
K140763,K140763
Product Code
FDI
Product Code Name
SNARE, FLEXIBLE
Public Device Record Key
71cb5439-e1ef-45d0-b640-8ac09e9b5936
Public Version Date
March 31, 2020
Public Version Number
6
DI Record Publish Date
September 17, 2016
Package DI Number
10816765012823
Quantity per Package
3
Contains DI Package
00816765012826
Package Discontinue Date
March 31, 2020
Package Status
Not in Commercial Distribution
Package Type
Box
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 51 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 902 |