Duns Number:780318028
Device Description: SculpSure laser assembly
Catalog Number
-
Brand Name
SculpSure laser assembly
Version/Model Number
100-7026-010
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
-
Product Code
PKT
Product Code Name
Laser for disruption of adipocyte cells for aesthetic use
Public Device Record Key
28c48f71-822c-49b8-b3d6-6b93c0f86f44
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
July 26, 2017
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 | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 154 |