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TITAN HIGH RESOLUTION ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030949
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2003
Days to Decision
12 days
Submission Type
Summary

TITAN HIGH RESOLUTION ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K030949
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/7/2003
Days to Decision
12 days
Submission Type
Summary