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IMRIS MR/X-RAY HEAD FIXATION DEVICE (HFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113748
510(k) Type
Traditional
Applicant
IMRIS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/23/2012
Days to Decision
93 days
Submission Type
Summary

IMRIS MR/X-RAY HEAD FIXATION DEVICE (HFD)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K113748
510(k) Type
Traditional
Applicant
IMRIS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
3/23/2012
Days to Decision
93 days
Submission Type
Summary