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NOBLUS™ Ultrasound Diagnostic System

Page Type
Cleared 510(K)
510(k) Number
K160559
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2016
Days to Decision
232 days
Submission Type
Summary

NOBLUS™ Ultrasound Diagnostic System

Page Type
Cleared 510(K)
510(k) Number
K160559
510(k) Type
Traditional
Applicant
HITACHI MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/2016
Days to Decision
232 days
Submission Type
Summary