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Discovery MR750 3.0T; Discovery MR750w 3.0T;Discovery MR450 1.5T; Discovery MR450w 1.5T; SIGNA Architect and SIGNA Artist

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163331
510(k) Type
Traditional
Applicant
GE Medical Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/17/2017
Days to Decision
109 days
Submission Type
Summary