Duns Number:544464442
Catalog Number
-
Brand Name
HOMEDICS
Version/Model Number
IPL-HH390
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
K161565,K161565
Product Code
OHT
Product Code Name
Light Based Over-The-Counter Hair Removal
Public Device Record Key
c0024ad6-ffb4-451b-93af-c790c82cbb98
Public Version Date
February 24, 2020
Public Version Number
4
DI Record Publish Date
March 31, 2017
Package DI Number
16970821120021
Quantity per Package
4
Contains DI Package
06970821120024
Package Discontinue Date
December 31, 2017
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 2 |