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MODIFICATION TO: DP-9900 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-9900

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053346
510(k) Type
Special
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
7 days
Submission Type
Summary

MODIFICATION TO: DP-9900 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-9900

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053346
510(k) Type
Special
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/9/2005
Days to Decision
7 days
Submission Type
Summary