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ALOKA SSD-5000 V5.0 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033311
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2003
Days to Decision
15 days
Submission Type
Summary

ALOKA SSD-5000 V5.0 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033311
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/29/2003
Days to Decision
15 days
Submission Type
Summary