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AIRIS ELITE MAGNETIC RESONANCE IMAGING DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032232
510(k) Type
Abbreviated
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2003
Days to Decision
70 days
Submission Type
Summary