Duns Number:006261481
Device Description: CATH AFAPRO23 AFA PRO 23 US
Catalog Number
-
Brand Name
Arctic Front Advance Pro™
Version/Model Number
AFAPRO23
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 04, 2019
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
P100010
Product Code
OAE
Product Code Name
Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation
Public Device Record Key
bfb907c3-c4d7-4250-b685-f895c1c7d087
Public Version Date
March 16, 2021
Public Version Number
2
DI Record Publish Date
January 21, 2019
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 | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |