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MAGNETIC RESONANCE DIAGNOSTIC DEVICE, AIRIS II

Page Type
Cleared 510(K)
510(k) Number
K984278
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
11 days
Submission Type
Summary

MAGNETIC RESONANCE DIAGNOSTIC DEVICE, AIRIS II

Page Type
Cleared 510(K)
510(k) Number
K984278
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1998
Days to Decision
11 days
Submission Type
Summary