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V8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211945
510(k) Type
Traditional
Applicant
Samsung Medison CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/8/2021
Days to Decision
77 days
Submission Type
Summary

V8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K211945
510(k) Type
Traditional
Applicant
Samsung Medison CO., LTD.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
9/8/2021
Days to Decision
77 days
Submission Type
Summary