Last synced on 25 January 2026 at 3:41 am

BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202405
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/7/2021
Days to Decision
139 days
Submission Type
Summary

BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19, BeneVision N22, BeneVision N1

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K202405
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/7/2021
Days to Decision
139 days
Submission Type
Summary