Last synced on 12 April 2024 at 11:04 pm

GE PROPELLER IMAGING OPTION FOR MRI

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K031230
510(k) Type
Traditional
Applicant
GE MEDICAL SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2003
Days to Decision
14 days
Submission Type
Summary