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ARIETTA 70/ARIETTA S70/ARIETTA V70 DIAGNOSTIC ULTRASOUND SCANNER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K134016
510(k) Type
Traditional
Applicant
HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2014
Days to Decision
88 days
Submission Type
Summary

ARIETTA 70/ARIETTA S70/ARIETTA V70 DIAGNOSTIC ULTRASOUND SCANNER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K134016
510(k) Type
Traditional
Applicant
HITACHI ALOKA MEDICAL,LTD. (HITACHI ALOKA MEDICAL
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/28/2014
Days to Decision
88 days
Submission Type
Summary