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Ablation Catheter, Renal Denervation

FDA product code QYI · Class 3 · Unknown

13
Registered devices
41
Adverse events
2
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-01-29ReCor Medical Inc.Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.
2026-01-29ReCor Medical Inc.Due to firm distributing a nonconforming product that supposed to be scrapped and not for human use.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.