K232943
- 510(k) number
- K232943
- Device name
- Hypodermic Needle-Pro® EDGE Safety Device with Low Dead Space Syringe
- Applicant
- Smiths Medical Asd, Inc. MN · US
- Product code
- QNQ — Low Dead Space Piston Syringe
- Decision date
- 2024-05-31
- Date received
- 2023-09-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
510(k) Summary (official FDA PDF): K232943.pdf
Official FDA record: K232943
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.