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GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X

Page Type
Cleared 510(K)
510(k) Number
K032656
510(k) Type
Special
Applicant
GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
63 days
Submission Type
Summary

GE LOGIQ 9 ULTRASOUND BT03/IQ, MODEL 2375600-X

Page Type
Cleared 510(K)
510(k) Number
K032656
510(k) Type
Special
Applicant
GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
63 days
Submission Type
Summary