Last synced on 23 February 2024 at 11:04 pm

FLEXART V3.1 SOFTWARE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962138
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/1996
Days to Decision
203 days
Submission Type
Summary