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SA8000 SE DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K043455
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
6 days
Submission Type
Summary

SA8000 SE DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K043455
510(k) Type
Traditional
Applicant
MEDISON CO., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
6 days
Submission Type
Summary