Last synced on 25 April 2025 at 11:05 pm

DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85/DC-86/DC-86S/DC-89/DC-TV/DC-TQ Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192152
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/13/2019
Days to Decision
126 days
Submission Type
Summary

DC-80/DC-80 PRO/DC-80 EXP/DC-80S/DC-85/DC-86/DC-86S/DC-89/DC-TV/DC-TQ Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K192152
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
12/13/2019
Days to Decision
126 days
Submission Type
Summary