Last synced on 25 April 2025 at 11:05 pm

Resona I8W, Resona I8, Resona I8 Exp, Resona I8S, Resona I8T, Resona IY,Resona I8 Easi, Eagus I8 Easi, Nuewa I8W, Nuewa I8, Nuewa I8 Exp, NuewaI8S, Nuewa I8T, Imagyn I8, Imagyn I8S, Imagyn I8T, Imagyn I8 Exp, Nuewa IY Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240115
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-medical Electronics Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/22/2024
Days to Decision
97 days
Submission Type
Summary

Resona I8W, Resona I8, Resona I8 Exp, Resona I8S, Resona I8T, Resona IY,Resona I8 Easi, Eagus I8 Easi, Nuewa I8W, Nuewa I8, Nuewa I8 Exp, NuewaI8S, Nuewa I8T, Imagyn I8, Imagyn I8S, Imagyn I8T, Imagyn I8 Exp, Nuewa IY Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K240115
510(k) Type
Traditional
Applicant
Shenzhen Mindray Bio-medical Electronics Co., LTD.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
4/22/2024
Days to Decision
97 days
Submission Type
Summary