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HD80 Series Ultrasound Diagnostic System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233841
510(k) Type
Traditional
Applicant
Qingdao Hisense Medical Equipment Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
164 days
Submission Type
Summary

HD80 Series Ultrasound Diagnostic System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K233841
510(k) Type
Traditional
Applicant
Qingdao Hisense Medical Equipment Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
5/16/2024
Days to Decision
164 days
Submission Type
Summary