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ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY

Page Type
Cleared 510(K)
510(k) Number
K930960
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1993
Days to Decision
250 days
Submission Type
Summary

ACCESS MAGNETIC RESONANCE DEVICE ACCESSORY

Page Type
Cleared 510(K)
510(k) Number
K930960
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1993
Days to Decision
250 days
Submission Type
Summary