Last synced on 6 December 2024 at 11:05 pm

1.5T SIGNA HDXT 3.0T SIGNA HDXT SIGNA VIBRANT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121676
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/20/2012
Days to Decision
105 days
Submission Type
Summary