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Sonosite PX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K213763
510(k) Type
Traditional
Applicant
FUJIFILM Sonosite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2021
Days to Decision
26 days
Submission Type
Summary

Sonosite PX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K213763
510(k) Type
Traditional
Applicant
FUJIFILM Sonosite, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/27/2021
Days to Decision
26 days
Submission Type
Summary