Last synced on 25 January 2026 at 3:41 am

Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221857
510(k) Type
Traditional
Applicant
Zhejiang Lude Technology Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
108 days
Submission Type
Summary

Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221857
510(k) Type
Traditional
Applicant
Zhejiang Lude Technology Development Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
10/13/2022
Days to Decision
108 days
Submission Type
Summary