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EchoPAC Software Only, EchoPAC Plug-in

Page Type
Cleared 510(K)
510(k) Number
K220940
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
113 days
Submission Type
Summary

EchoPAC Software Only, EchoPAC Plug-in

Page Type
Cleared 510(K)
510(k) Number
K220940
510(k) Type
Traditional
Applicant
GE Medical Systems Ultrasound and Primary Care Diagnostics,
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/2022
Days to Decision
113 days
Submission Type
Summary