Last synced on 30 November 2024 at 11:09 am

MRI ULTRAVIEW

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915260
510(k) Type
Traditional
Applicant
A&E SPECIALTY FABRICATORS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1992
Days to Decision
118 days
Submission Type
Statement