K240165
- 510(k) number
- K240165
- Device name
- Aneroid Sphygmomanometer with Stethoscope; Aneroid Sphygmomanometer
- Applicant
- Wenzhou Longwan Medical Device Factory CN
- Product code
- DXQ — Blood Pressure Cuff
- Decision date
- 2024-03-20
- Date received
- 2024-01-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
510(k) Summary (official FDA PDF): K240165.pdf
Official FDA record: K240165
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.