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SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102390
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
88 days
Submission Type
Summary

SONOSITE NANOMAXX SERIES ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K102390
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2010
Days to Decision
88 days
Submission Type
Summary