Duns Number:407522184
Catalog Number
92-50-3G
Brand Name
Scleral Buckling Products: Style 506G, 3.0mm x 5.0mm Grooved Sponge
Version/Model Number
92-50-3G
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
K023481,K023481
Product Code
HQX
Product Code Name
Implant, Orbital, Extra-Ocular
Public Device Record Key
4dcee45e-f78b-4edb-9e2d-1d71505c2d51
Public Version Date
December 22, 2021
Public Version Number
6
DI Record Publish Date
September 24, 2015
Package DI Number
18717872014583
Quantity per Package
5
Contains DI Package
08717872014586
Package Discontinue Date
-
Package Status
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 | 203 |
2 | A medical device with a moderate to high risk that requires special controls. | 149 |