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DUOFLEX COIL SUITE (1.5T)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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