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DC-8/DC-8 PRO/DC-8, CV/DC-8, EXP/DC-8S DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123185
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2012
Days to Decision
23 days
Submission Type
Summary

DC-8/DC-8 PRO/DC-8, CV/DC-8, EXP/DC-8S DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123185
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
11/2/2012
Days to Decision
23 days
Submission Type
Summary