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

Ablation Catheter, Renal Denervation

Unknown
FDA source (opens on fda.gov)

QYI is the FDA product code for Ablation Catheter, Renal Denervation, a class III device type. FDA's definition for this code reads: "For denervating the renal nerves to lower blood pressure". As of , FDA records hold no 510(k) clearances under this code and 2 recalls.

Classification record

Product code
QYI
Device name
Ablation Catheter, Renal Denervation
FDA definition
For denervating the renal nerves to lower blood pressure
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
2

Companies listing this code with FDA

Companies whose registered establishments list this code