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DUOFLEX COIL SUITE (1.5T)

Page Type
Cleared 510(K)
510(k) Number
K130706
510(k) Type
Traditional
Applicant
MR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2013
Days to Decision
132 days
Submission Type
Summary

DUOFLEX COIL SUITE (1.5T)

Page Type
Cleared 510(K)
510(k) Number
K130706
510(k) Type
Traditional
Applicant
MR INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/25/2013
Days to Decision
132 days
Submission Type
Summary