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Sonosite LX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K233597
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2023
Days to Decision
28 days
Submission Type
Summary

Sonosite LX Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K233597
510(k) Type
Traditional
Applicant
FUJIFILM SonoSite Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/6/2023
Days to Decision
28 days
Submission Type
Summary