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GE ECHOPAC

Page Type
Cleared 510(K)
510(k) Number
K123894
510(k) Type
Traditional
Applicant
GE VINGMED ULTRASOUND AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2013
Days to Decision
42 days
Submission Type
Summary

GE ECHOPAC

Page Type
Cleared 510(K)
510(k) Number
K123894
510(k) Type
Traditional
Applicant
GE VINGMED ULTRASOUND AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/29/2013
Days to Decision
42 days
Submission Type
Summary