Hewlett-Packard M1205A Viridia 24 CT

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K981376 ↗

FDA Product Code

DSI

Device Class

Class II

Regulation

21 CFR Part 870.1025

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K922184 Active Cleared 30 Jul 1992

• Medical Diag. Ultrasound Instr. 77065

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  Class I

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  Class II

  FDA 510(k) K781360 Active Cleared 7 Sep 1978

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