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GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K993364
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1999
Days to Decision
30 days
Submission Type
Summary

GE LOGIQ 700 WITH CODED EXCITATION MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K993364
510(k) Type
Special
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/5/1999
Days to Decision
30 days
Submission Type
Summary