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Sonosite PX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K200964
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2020
Days to Decision
28 days
Submission Type
Summary

Sonosite PX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K200964
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2020
Days to Decision
28 days
Submission Type
Summary