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FLEXART,FLEXART/HYPER, VISART, VISART/HYPER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K983110
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/1999
Days to Decision
174 days
Submission Type
Summary