Duns Number:830016148
Device Description: 1820 FACE MASK, EARLOOP, FLUID RESISTANT
Catalog Number
1820
Brand Name
3M™
Version/Model Number
1820
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
-
Product Code
FXX
Product Code Name
Mask, surgical
Public Device Record Key
1b6857fd-0ff6-4f94-96c9-4f79cfcfcb38
Public Version Date
March 11, 2021
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
50707387256031
Quantity per Package
12
Contains DI Package
30707387256037
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| 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 |