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ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032875
510(k) Type
Traditional
Applicant
ALOKA CO. LTD USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2003
Days to Decision
15 days
Submission Type
Summary

ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032875
510(k) Type
Traditional
Applicant
ALOKA CO. LTD USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/2003
Days to Decision
15 days
Submission Type
Summary