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Aplio i900/i800/i700 Diagnostic Ultrasound System, V2.1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163702
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/30/2017
Days to Decision
152 days
Submission Type
Summary

Aplio i900/i800/i700 Diagnostic Ultrasound System, V2.1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K163702
510(k) Type
Traditional
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
5/30/2017
Days to Decision
152 days
Submission Type
Summary