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Upper Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221212
510(k) Type
Traditional
Applicant
Shenzhen Yolanda Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/26/2022
Days to Decision
121 days
Submission Type
Statement

Upper Arm Blood Pressure Monitor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221212
510(k) Type
Traditional
Applicant
Shenzhen Yolanda Technology Co., Ltd
Country
China
FDA Decision
Substantially Equivalent
Decision Date
8/26/2022
Days to Decision
121 days
Submission Type
Statement