Last synced on 14 November 2025 at 11:06 pm

SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071134
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2007
Days to Decision
15 days
Submission Type
Summary

SONOSITE MAXX SERIES DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K071134
510(k) Type
Traditional
Applicant
SONOSITE,INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2007
Days to Decision
15 days
Submission Type
Summary