Last synced on 14 November 2025 at 11:06 pm

FLEXART QD HEAD/NECK COIL

Page Type
Cleared 510(K)
510(k) Number
K961391
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1996
Days to Decision
90 days
Submission Type
Summary

FLEXART QD HEAD/NECK COIL

Page Type
Cleared 510(K)
510(k) Number
K961391
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/9/1996
Days to Decision
90 days
Submission Type
Summary