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SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101757
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2010
Days to Decision
50 days
Submission Type
Summary

SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM, SONOSITE MAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101757
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/2010
Days to Decision
50 days
Submission Type
Summary