Duns Number:187502109
Device Description: Fiber Optic Cable
Catalog Number
0233-050-300
Brand Name
AIM SafeLight
Version/Model Number
0233050300
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
July 01, 2022
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
-
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
K142310
Product Code
OWN
Product Code Name
Confocal optical imaging
Public Device Record Key
83e120d9-0ebb-457d-854d-aaaf84cae4b1
Public Version Date
July 01, 2022
Public Version Number
6
DI Record Publish Date
September 23, 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 | 2188 |
2 | A medical device with a moderate to high risk that requires special controls. | 3183 |
U | Unclassified | 60 |