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NEURO II-SE, MODELS: OR-DR-OR, OR-MB

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071099
510(k) Type
Traditional
Applicant
IMRIS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/22/2007
Days to Decision
33 days
Submission Type
Summary