Last synced on 25 April 2025 at 11:05 pm

Sonosite PX Ultrasound System, Sonosite SII Ultrasound System, Sonosite iViz Ultrasound System, Sonosite X-Porte Ultrasound System, Sonosite Edge II Ultrasound System, Sonosite Maxx Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202160
510(k) Type
Special
Applicant
FUJIFILM SonoSite Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2020
Days to Decision
29 days
Submission Type
Summary

Sonosite PX Ultrasound System, Sonosite SII Ultrasound System, Sonosite iViz Ultrasound System, Sonosite X-Porte Ultrasound System, Sonosite Edge II Ultrasound System, Sonosite Maxx Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202160
510(k) Type
Special
Applicant
FUJIFILM SonoSite Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/1/2020
Days to Decision
29 days
Submission Type
Summary