Duns Number:532685716
Device Description: Refurbished, CO2RE System for US, Packaged
Catalog Number
FG70412USR
Brand Name
Refurbished, CO2RE System for US, Packaged
Version/Model Number
FG70412USR
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
-
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
K151655
Product Code
GEX
Product Code Name
Powered Laser Surgical Instrument
Public Device Record Key
7cfaab67-f8a7-43f0-882d-d00b15dce58e
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
June 01, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 194 |