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BeneVision N Series Patient Monitors (Including BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19. BeneVision N22, BeneVision N1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182075
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-medical Electronics Co., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/10/2018
Days to Decision
131 days
Submission Type
Summary

BeneVision N Series Patient Monitors (Including BeneVision N12, BeneVision N15, BeneVision N17, BeneVision N19. BeneVision N22, BeneVision N1)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182075
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-medical Electronics Co., LTD.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/10/2018
Days to Decision
131 days
Submission Type
Summary