Last synced on 9 May 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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