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AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K980691
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1998
Days to Decision
77 days
Submission Type
Summary

AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K980691
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1998
Days to Decision
77 days
Submission Type
Summary