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SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)

Page Type
Cleared 510(K)
510(k) Number
K053069
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2005
Days to Decision
15 days
Submission Type
Summary

SONOSITE MICROMAXX DIAGNOSTIC ULTRASOUND SYSTEM (C3 SERIES)

Page Type
Cleared 510(K)
510(k) Number
K053069
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/2005
Days to Decision
15 days
Submission Type
Summary