Last synced on 14 November 2025 at 11:06 pm

ALOKA ARIETTA 850

Page Type
Cleared 510(K)
510(k) Number
K173739
510(k) Type
Traditional
Applicant
Hitachi Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2018
Days to Decision
83 days
Submission Type
Summary

ALOKA ARIETTA 850

Page Type
Cleared 510(K)
510(k) Number
K173739
510(k) Type
Traditional
Applicant
Hitachi Healthcare Americas Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/28/2018
Days to Decision
83 days
Submission Type
Summary