Duns Number:830016148
Device Description: 3M™ Cavilon™ No Sting Barrier Film Wipes, 0.75 ML, Carton of 100 Wipes, 3342K
Catalog Number
3342K
Brand Name
3M™ Cavilon™
Version/Model Number
3342K
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"
Yes
For Single-Use
Yes
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
K955103,K955103,K955103
Product Code
KMF
Product Code Name
Bandage, liquid
Public Device Record Key
76c0fb7f-048b-4ce6-987c-1845ffd47b40
Public Version Date
May 16, 2019
Public Version Number
1
DI Record Publish Date
May 08, 2019
Package DI Number
50707387787092
Quantity per Package
12
Contains DI Package
30707387787098
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 274 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 444 |
| U | Unclassified | 7 |