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ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K920374
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1992
Days to Decision
64 days
Submission Type
Statement

ALOKA 650CL DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K920374
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/2/1992
Days to Decision
64 days
Submission Type
Statement