Last synced on 25 January 2026 at 3:41 am

AIRIS MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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