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GE ECHOPAC MODEL BT10

Page Type
Cleared 510(K)
510(k) Number
K101324
510(k) Type
Traditional
Applicant
GE VINGMED ULTRASOUND AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
147 days
Submission Type
Summary

GE ECHOPAC MODEL BT10

Page Type
Cleared 510(K)
510(k) Number
K101324
510(k) Type
Traditional
Applicant
GE VINGMED ULTRASOUND AS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2010
Days to Decision
147 days
Submission Type
Summary