Last synced on 25 April 2025 at 11:05 pm

MX7/MX7T/Vaus7/Zeus/ME7/Anesus ME7/Anesus ME7T/MX8/MX8T/Vaus8/ME8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212900
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/5/2021
Days to Decision
53 days
Submission Type
Summary

MX7/MX7T/Vaus7/Zeus/ME7/Anesus ME7/Anesus ME7T/MX8/MX8T/Vaus8/ME8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212900
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/5/2021
Days to Decision
53 days
Submission Type
Summary