Last synced on 25 April 2025 at 11:05 pm

Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173090
510(k) Type
Traditional
Applicant
Toshiba Medical Systems Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
1/11/2018
Days to Decision
104 days
Submission Type
Summary

Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V2.4

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K173090
510(k) Type
Traditional
Applicant
Toshiba Medical Systems Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
1/11/2018
Days to Decision
104 days
Submission Type
Summary