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AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012154
510(k) Type
Traditional
Applicant
AURORA IMAGING TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2001
Days to Decision
70 days
Submission Type
Summary

AURORA MAGNETIC RESONANCE DIAGNOSTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012154
510(k) Type
Traditional
Applicant
AURORA IMAGING TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2001
Days to Decision
70 days
Submission Type
Summary