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MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K903319
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
23 days

MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K903319
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1990
Days to Decision
23 days