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AQUILION PRIME, V5.00

Page Type
Cleared 510(K)
510(k) Number
K130645
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2013
Days to Decision
87 days
Submission Type
Summary

AQUILION PRIME, V5.00

Page Type
Cleared 510(K)
510(k) Number
K130645
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/6/2013
Days to Decision
87 days
Submission Type
Summary