Duns Number:801895244
Device Description: Fischer Cone Biopsy Excisor; Small Wide Angle
Catalog Number
-
Brand Name
Fischer Cone Biopsy Excisor
Version/Model Number
900-157
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
K061651,K061651
Product Code
HGI
Product Code Name
Electrocautery, Gynecologic (And Accessories)
Public Device Record Key
3dff1c2b-893a-4431-b2d9-0d564697dda4
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
August 16, 2016
Package DI Number
20888937003769
Quantity per Package
5
Contains DI Package
00888937003765
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 | 29 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1471 |
| 3 | A medical device with high risk that requires premarket approval | 2 |