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ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081843
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
15 days
Submission Type
Summary

ULTRASOUND DATA ANALYSIS SYSTEM, MODEL DAS-RS1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081843
510(k) Type
Traditional
Applicant
ALOKA CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/15/2008
Days to Decision
15 days
Submission Type
Summary