Duns Number:043618763
Catalog Number
-
Brand Name
Acculite EndoOcular
Version/Model Number
Illum/Sm Plug, 20ga 45°, SMA 906, 200µm
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 20, 2019
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
K931784,K931784
Product Code
HQF
Product Code Name
Laser, Ophthalmic
Public Device Record Key
e7f67908-b654-453a-8a49-4aea3b3b4afa
Public Version Date
May 21, 2019
Public Version Number
4
DI Record Publish Date
September 25, 2016
Package DI Number
17290109140800
Quantity per Package
10
Contains DI Package
07290109140803
Package Discontinue Date
May 20, 2019
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 48 |