Last synced on 25 April 2025 at 11:05 pm

M6/M6T/M6 EXP/M6S/M6 PRO/M5 EXP/M55/M58 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171579
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/18/2017
Days to Decision
140 days
Submission Type
Summary

M6/M6T/M6 EXP/M6S/M6 PRO/M5 EXP/M55/M58 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171579
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/18/2017
Days to Decision
140 days
Submission Type
Summary