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ALOKA MODEL SSD-4000 DIAGNOSTIC ULTRASOUND SYSTEM W/OPTIONAL SONOREAL 3D SYSTEM ACCESSORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040719
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
7 days
Submission Type
Summary

ALOKA MODEL SSD-4000 DIAGNOSTIC ULTRASOUND SYSTEM W/OPTIONAL SONOREAL 3D SYSTEM ACCESSORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040719
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/26/2004
Days to Decision
7 days
Submission Type
Summary