Duns Number:175697908
Device Description: The Invuity Single Fiber Optic Cable and Invuity Bifurcated Fiber Optic Cable are intended
Catalog Number
110001
Brand Name
Invuity® Fiber Optic Cable
Version/Model Number
Bifurcated
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"
Yes
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
K090070
Product Code
FST
Product Code Name
Light, Surgical, Fiberoptic
Public Device Record Key
679625ca-a8c1-49f7-a798-cb478711c4e1
Public Version Date
April 24, 2020
Public Version Number
4
DI Record Publish Date
September 22, 2016
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 |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 10 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 28 |