Duns Number:001951946
Device Description: Intense Pulse Light OTC hair removal device
Catalog Number
-
Brand Name
Remington
Version/Model Number
IPL7510
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K141583,K141583
Product Code
ONF
Product Code Name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Public Device Record Key
9e491691-6cfc-43e1-b8f6-ea90804f519b
Public Version Date
October 19, 2021
Public Version Number
2
DI Record Publish Date
September 26, 2019
Package DI Number
10074590544500
Quantity per Package
4
Contains DI Package
00074590544503
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
cardboard
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 16 |