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Arm-type Fully Automatic Digital Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231303
510(k) Type
Traditional
Applicant
Joytech Healthcare Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/26/2024
Days to Decision
266 days
Submission Type
Summary

Arm-type Fully Automatic Digital Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231303
510(k) Type
Traditional
Applicant
Joytech Healthcare Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/26/2024
Days to Decision
266 days
Submission Type
Summary