Last synced on 23 February 2024 at 11:04 pm

MAGNETIC RESONANCE DIAGNOSTIC DEVICE, VERSION 5.0 OPERATING SYSTEM SOFTWARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K984274
510(k) Type
Traditional
Applicant
HITACHI MEDICAL SYSTEMS AMERICA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1999
Days to Decision
56 days
Submission Type
Summary