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AURORA IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K950837
510(k) Type
Traditional
Applicant
ADVANCED MAMMOGRAPHY SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1996
Days to Decision
367 days
Submission Type
Summary