Diasonics SpA 5.O 27mm Probe

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K864758 ↗

FDA Product Code

ITX

Device Class

Class II

Regulation

21 CFR Part 892.1570

Advisory Committee

Radiology

FDA Decision

SESE Substantially Equivalent

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  Class II

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  FDA 510(k) K903562 Active Cleared 2 Mar 1992

• Diasonics Drf-200 Ultrasound Imaging System

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  FDA 510(k) K851860 Active Cleared 31 Oct 1985

• Diasonics, Berger Stereotactic Neorobiopsy

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  FDA 510(k) K851973 Active Cleared 26 Jul 1985

• Adms Transrectal 7.5 Mhz Probe

  Class II

  FDA 510(k) K870967 Active Cleared 29 Sep 1987

• Cfm-800 Color Flow Mapping System

  Class II

  FDA 510(k) K924079 Active Cleared 28 Sep 1993

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