Last synced on 25 January 2026 at 3:41 am

TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043452
510(k) Type
Traditional
Applicant
Sonosite,Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
6 days
Submission Type
Summary

TITAN HIGH RESOLUTION ULTRASOUND SYSTEM AND SONOSITE ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043452
510(k) Type
Traditional
Applicant
Sonosite,Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/21/2004
Days to Decision
6 days
Submission Type
Summary