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Results for “MODIFICATION TO: AURORA”

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4 devices foundsorted by relevance

  • Modification To: Aurora

    Aurora Imaging Technology, Inc.,United States(FDA applicant) Group of variants
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modification To Aurora Mri System

    Aurora Imaging Technology, Inc.,United States(FDA applicant)
    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Modification To Aurora Ds

    Syneron Medical Ltd,FDA registration: United States
    Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 1-4 of 4