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BeneVision Central Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220058
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/1/2022
Days to Decision
146 days
Submission Type
Summary

BeneVision Central Monitoring System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220058
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., LTD
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/1/2022
Days to Decision
146 days
Submission Type
Summary