Duns Number:001137280
Device Description: Post-OP Sinus Pack K9 with string
Catalog Number
Q770532
Brand Name
FABCO
Version/Model Number
Q770532
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
-
Product Code
EMX
Product Code Name
Balloon, Epistaxis
Public Device Record Key
cc38ffa3-3d9a-4272-b557-5b05296d2b68
Public Version Date
December 21, 2020
Public Version Number
3
DI Record Publish Date
March 05, 2018
Package DI Number
50634303800576
Quantity per Package
10
Contains DI Package
30634303800572
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Dispenser Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 75 |
2 | A medical device with a moderate to high risk that requires special controls. | 5 |