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FLEXART(TM) QD C-SPINE COIL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945665
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/1995
Days to Decision
140 days
Submission Type
Summary