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Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V3.1

Page Type
Cleared 510(K)
510(k) Number
K182679
510(k) Type
Traditional
Applicant
Canon Medical Systems Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/31/2018
Days to Decision
35 days
Submission Type
Summary

Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V3.1

Page Type
Cleared 510(K)
510(k) Number
K182679
510(k) Type
Traditional
Applicant
Canon Medical Systems Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/31/2018
Days to Decision
35 days
Submission Type
Summary