Duns Number:117844489
Device Description: OtoClear Ear Wax Removal
Catalog Number
701
Brand Name
OtoClear® Ear Wax Removal
Version/Model Number
701
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
-
Product Code
KCP
Product Code Name
SYRINGE, ENT
Public Device Record Key
38d15560-7bf7-4176-b8ad-6daf90587dae
Public Version Date
January 17, 2022
Public Version Number
1
DI Record Publish Date
January 07, 2022
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 | 61 |
2 | A medical device with a moderate to high risk that requires special controls. | 27 |