Last synced on 12 October 2025 at 8:21 pm

SonoSite SII Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160734
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2016
Days to Decision
19 days
Submission Type
Summary

SonoSite SII Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K160734
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/5/2016
Days to Decision
19 days
Submission Type
Summary