Duns Number:801895244
Device Description: LEEP Square Condyloma Electrode 5.5cm Shaft; 15 Degree Bend
Catalog Number
-
Brand Name
LEEP Square Condyloma Electrode
Version/Model Number
S1004
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
K905747,K905747
Product Code
HGI
Product Code Name
Electrocautery, Gynecologic (And Accessories)
Public Device Record Key
c1ea6585-a119-4d24-ab0d-78af5a3a3f4c
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
August 15, 2016
Package DI Number
20888937010866
Quantity per Package
5
Contains DI Package
00888937010862
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 |