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GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992208
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1999
Days to Decision
12 days
Submission Type
Summary

GE LOGIQ 200 MD DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K992208
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1999
Days to Decision
12 days
Submission Type
Summary