Last synced on 25 April 2025 at 11:05 pm

DC-8/ DC-8 PRO/ DC-8 CV/ DC-8 EXP/ DC-8S DIAGNOSTIC ULTRASOUND SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132341
510(k) Type
Traditional
Applicant
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/15/2013
Days to Decision
20 days
Submission Type
Summary

DC-8/ DC-8 PRO/ DC-8 CV/ DC-8 EXP/ DC-8S DIAGNOSTIC ULTRASOUND SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K132341
510(k) Type
Traditional
Applicant
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/15/2013
Days to Decision
20 days
Submission Type
Summary