510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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OADClass III

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

Unknown
FDA source (opens on fda.gov)

OAD is the FDA product code for Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter, a class III device type. FDA's definition for this code reads: "For the treatment of atrial flutter". As of , FDA records hold no 510(k) clearances under this code and 22 recalls.

Classification record

Product code
OAD
Device name
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA definition
For the treatment of atrial flutter.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
Yes
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
22

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 37 companies shown, in name order