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FLEXART QD BODY COIL

Page Type
Cleared 510(K)
510(k) Number
K944662
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1995
Days to Decision
126 days
Submission Type
Summary

FLEXART QD BODY COIL

Page Type
Cleared 510(K)
510(k) Number
K944662
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/1995
Days to Decision
126 days
Submission Type
Summary