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AIRIS II MAGNETIC RESONANCE DIAGNOSTIC DEVICE,INTERVENTIONAL MR PACKAGE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984280
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1999
Days to Decision
70 days
Submission Type
Summary