Duns Number:053468385
Catalog Number
-
Brand Name
Applicator PL 400 400 - 720 nm
Version/Model Number
9APP7749-CNDL
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
K150907
Product Code
GEX
Product Code Name
Powered Laser Surgical Instrument
Public Device Record Key
bf57ba1e-98dd-4871-8f17-b8083cef2ddc
Public Version Date
October 12, 2022
Public Version Number
2
DI Record Publish Date
January 15, 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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 122 |