Last synced on 23 February 2024 at 11:04 pm

IFIS-SA INTEGRATED FUCTIONAL IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003899
510(k) Type
Traditional
Applicant
MRI DEVICES CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/15/2001
Days to Decision
87 days
Submission Type
Summary