Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201— 510(k) K221857
Substantially EquivalentZhejiang Lude Technology Development Co., Ltd.
FDA 510(k) clearance K221857 for Aneroid sphygmomanometer with stethoscope, QL-50, Aneroid sphygmomanometer, QL-20, Aneroid sphygmomanometer, QL-201, Substantially Equivalent on 2022-10-13. Applicant: Zhejiang Lude Technology Development Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Zhejiang Lude Technology Development Co., Ltd.
- Product code
- Code DXQ
- Device class
- Class 2
- Regulation
- 21 CFR 870.1120
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Wenzhou, CN
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Data sourced from openFDA. This site is unofficial and independent of the FDA.