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SONOSITE MAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082098
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2008
Days to Decision
31 days
Submission Type
Summary

SONOSITE MAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K082098
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/2008
Days to Decision
31 days
Submission Type
Summary