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ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093488
510(k) Type
Traditional
Applicant
Aloka Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2009
Days to Decision
10 days
Submission Type
Summary

ALOKA PROSOUND ALPHA 6 DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K093488
510(k) Type
Traditional
Applicant
Aloka Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/20/2009
Days to Decision
10 days
Submission Type
Summary