Last synced on 24 May 2024 at 11:04 pm

MAGNETOM Aera

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182299
510(k) Type
Traditional
Applicant
Siemens Medical Solutions USA Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2018
Days to Decision
63 days
Submission Type
Summary