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Variants of ALOKA ARIETTA 850 by Hitachi Healthcare Americas Corporation

3 variants

  • Aloka Arietta 850 Open recall

    Hitachi Healthcare Americas Corporation,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aloka Arietta 850 Open recall

    Hitachi Healthcare Americas Corporation,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Aloka Arietta 850 Open recall

    Hitachi Healthcare Americas Corporation,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II

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