Duns Number:027680821
Device Description: Intended to be used as an anti-fog agent for endoscopic camera lenses
Catalog Number
-
Brand Name
Dr. Fog® Solution With Sponge
Version/Model Number
DF-3100
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
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K932449,K932449,K932449
Product Code
OCT
Product Code Name
Anti fog solution and accessories, endoscopy
Public Device Record Key
a3a51099-4b4f-402c-b917-7675f3c2f9df
Public Version Date
March 04, 2021
Public Version Number
5
DI Record Publish Date
September 17, 2016
Package DI Number
20887761000067
Quantity per Package
15
Contains DI Package
10887761000060
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 952 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 494 |