Duns Number:204046564
Catalog Number
-
Brand Name
Lucent IPL
Version/Model Number
ESM-9200IL
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
-
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
K193072
Product Code
ONF
Product Code Name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Public Device Record Key
16ec24dc-551f-47cf-9613-8123bf3e5c72
Public Version Date
June 09, 2021
Public Version Number
1
DI Record Publish Date
June 01, 2021
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 | 8 |
2 | A medical device with a moderate to high risk that requires special controls. | 10 |