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PROSOUND F37 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL: PROSOUND F37

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122341
510(k) Type
Traditional
Applicant
Hitachi Aloka Medical, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2012
Days to Decision
55 days
Submission Type
Summary

PROSOUND F37 DIAGNOSTIC ULTRASOUND SYSTEM, MODEL: PROSOUND F37

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122341
510(k) Type
Traditional
Applicant
Hitachi Aloka Medical, Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/26/2012
Days to Decision
55 days
Submission Type
Summary