Akonya Eliminator Mechanical Thrombectomy Device, Model El 10060060

No FDA recalls found in the data synced 11 Oct 2026.

510(k) Number

K030504 ↗

FDA Product Code

MCW

Device Class

Class II

Regulation

21 CFR Part 870.4875

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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• Supera Veritas Interwoven Self-Expanding Nitinol Stent Transhepatic Biliary System

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  FDA 510(k) K122546 Active Cleared 7 Dec 2012

• Supera Veritas

  Class II

  FDA 510(k) K130591 Active Cleared 2 May 2013

• Akonya Eliminator Mechanical Thrombectomy Device, Model EL10060060

  Class II

  FDA 510(k) K041374 Active Cleared 2 Mar 2005

• Texan Longhorn Foreign Body Retrieval Device, Model TX30120060

  Class II

  FDA 510(k) K050926 Active Cleared 9 May 2005

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