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MODIFICATION TO AURORA MRI SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073425
510(k) Type
Traditional
Applicant
AURORA IMAGING TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2008
Days to Decision
288 days
Submission Type
Summary

MODIFICATION TO AURORA MRI SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K073425
510(k) Type
Traditional
Applicant
AURORA IMAGING TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/16/2008
Days to Decision
288 days
Submission Type
Summary